Skip to main content

SYSTEMATIC REVIEW article

Front. Oncol. , 31 March 2025

Sec. Molecular and Cellular Oncology

Volume 15 - 2025 | https://doi.org/10.3389/fonc.2025.1562621

This article is part of the Research Topic Crosstalk between Lung Cancer and Fibrosis: Pathogenesis and Therapeutic Strategies View all 5 articles

The rising influence of lipid metabolism in lung cancer: a global research perspective

Chaoqun Wang&#x;Chaoqun Wang1†Ming Lei&#x;Ming Lei2†Wei Wang&#x;Wei Wang3†Yuanyuan JiangYuanyuan Jiang1Jiefeng ZhangJiefeng Zhang4Yi ZhangYi Zhang5Bin Zhao*Bin Zhao6*Wenyang Wang*Wenyang Wang1*
  • 1Department of Clinical Laboratory, The Affiliated Taian City Central Hospital of Qingdao University, Taian, China
  • 2Department of Minimally Invasive Oncology, The Affiliated Taian City Central Hospital of Qingdao University, Taian, China
  • 3Department of Intensive Care Medicine, The Affiliated Taian City Central Hospital of Qingdao University, Taian, China
  • 4Department of Emergency Medicine, The Affiliated Taian City Central Hospital of Qingdao University, Taian, China
  • 5Department of Gynecology, The Affiliated Taian City Central Hospital of Qingdao University, Taian, China
  • 6Department of Pediatric Surgery, The Affiliated Taian City Central Hospital of Qingdao University, Taian, China

Background: Lung cancer is a prevalent malignant neoplasm globally and the leading cause of cancer-related mortality, posing a significant threat to human health and imposing a considerable societal burden. Researchers have recently focused more on lipid metabolism in lung cancer. However, to date, there has been no bibliometric analysis of lung cancer in relation to lipid metabolism. This study used bibliometric methods to analyze the link between lipid metabolism and lung cancer.

Methods: Publications on lung cancer and lipid metabolism from 1995 to 2024 were sourced from the Web of Science Core Collection (WoSCC). The Microsoft Excel, R-bibliometrix, CiteSpace, and VOSviewer software were used to analyze and visualize the data.

Results: In this study, a total of 535 publications were identified, with a marked increase in the number of publications observed post-2016. Both China and the United States exerted substantial influence in this domain. Notably, the Chinese Academy of Sciences and Huazhong University of Science and Technology have demonstrated leadership in various aspects of lipid metabolism research related to lung cancer. Professor Ana Ramirez de Molina and Frontiers in Oncology were the most productive authors and journals respectively. Besides, keywords like “lipid metabolism”, “lung cancer”, “expression”, “metabolism” and “growth” were central to current research and are expected to continue driving future trends in lung cancer and metabolism studies.

Conclusions: Research on the relationship between lung cancer and lipid metabolism was still in its early stages. Targeting lipid metabolism in lung cancer represented a promising therapeutic strategy, as inhibiting key enzymes involved in lipid biosynthesis and uptake has the potential to impede cancer progression and mitigate drug resistance. This bibliometric study was the first to thoroughly summarize research trends and developments in this area over the past thirty years, providing scholars with updated insights and identifying future research directions.

1 Introduction

Lung cancer is one of the most common malignant tumors worldwide and the leading cause of cancer-related deaths, posing a serious threat to human health (1). The global burden of lung cancer was significant, with approximately 2.48 million new cases and 1.8 million deaths reported in 2022 alone (2, 3). Furthermore, lung cancer is the most diagnosed malignancy and the leading cause of cancer-related mortality worldwide. The incidence and mortality rates of lung cancer vary according to sex, geographic regions, and socioeconomic factors. Projections suggest that if current trends continue, the number of new cases could rise to 4.62 million, with 3.55 million deaths anticipated by 2050 (3).

Lipid metabolism has emerged as a significant research hotspot in the field of cancer biology, particularly in identifying new metabolic targets for lung cancer treatment (4). The alteration of lipid metabolism is a defining characteristic of lung cancer, significantly contributing to tumor development, progression, and therapeutic resistance (5). Recent research has underscored the significance of lipid metabolic pathways and their potential as targets for therapeutic intervention in lung cancer (6). By understanding the complex interactions between lipid metabolism and cancer biology, researchers can devise targeted therapies that leverage the metabolic susceptibilities of lung cancer cells. This strategy has the potential to enhance treatment outcomes and offer renewed hope for patients afflicted with lung cancer (7, 8).

Bibliometrics is an emerging method for analyzing literature, offering a systematic approach to understanding research trends and hotspots across various fields (9). Despite its growing application, there remains a gap in comprehensive bibliometric studies specifically focusing on the intersection of lung cancer and lipid metabolism. Consequently, conducting a bibliometric analysis focused on lung cancer and lipid metabolism provided valuable insights into the current research landscape, identified leading researchers and institutions, and highlighted emerging trends and future directions. Through the application of bibliometric methodologies, researchers could systematically evaluate the role of lipid metabolism in lung cancer and explore innovative therapeutic strategies designed to improve patient outcomes.

2 Data acquisition and methods

2.1 Data collection and processing

The data were collected from the Web of Science core collection Databases. The search terms were presented in the following manner: TS=((lipid metabolism or fatty acid metabolism) AND (Lung Cancer or Pulmonary Cancer)) and the time range from January 1, 1995 to December 31, 2024. As reported previously (10), these records were downloaded in text format, encompassing details such as the author, title, summary, and citation information. The above results were uploaded to CiteSpace v6.2.R2 (https://citespace.podia.com) and Microsoft Excel 2021 for further analysis (10).

2.2 Bibliometric analysis

VOSviewer(version 1.6.19), CiteSpace, and R (version 4.4.2) were used for the statistical computing and graphics. VOSviewer utilized data from the Web of Science Core Collection (WoSCC) to construct bibliometric maps, enabling a detailed and comprehensive analysis of these maps with consideration of collaborative data (11, 12). CiteSpace was designed to analyze the underlying knowledge structures within scientific literature and to visualize the collected data (12).

3 Results

3.1 Global trends of publication

The annual publication count serves as a key indicator of the trend in the progression of scientific knowledge within a specific field. A total of 535 publications were rigorously selected based on predefined inclusion criteria (Figure 1A). Analysis of the temporal distribution of these publications revealed two distinct phases in the annual trend. From 1995 to 2015, the number of publications fluctuated within a narrow range of 0 to 20. Since 2016, there has been a significant upward trend in the number of publications. Notably, in 2024, the number of publications reached its highest point, totaling 89, which constitutes 16.64% of the total selected publications.

Figure 1
www.frontiersin.org

Figure 1. Global trends of publication. (A) Annual publications from 1995 to 2024. (B) Fields of the WoS categories associated with the lipid metabolism in lung cancer.

The focal point of this study can be elucidated through a comprehensive analysis of the research field. As illustrated in Figure 1B, the highest-ranked fields relevant to this investigation were highlighted. Specifically, the primary domains involved in this study were “Oncology” (200 publications), followed by “Biochemistry and Molecular Biology” (94 publications), and “Cell Biology” (69 publications).

3.2 Analysis of journals

Table 1 listed the top 10 journals for co-citation in the field of lipid metabolism in lung cancer, with Frontiers in Oncology ranking first. This journal is renowned for its significant contributions to cancer research, focusing on publishing high-quality research articles and advancing the understanding of oncology. Cancer Research, which has a higher impact factor among oncology journals, highlights the critical importance and recognition of lipid metabolism in lung cancer as a key area of contemporary research.

Table 1
www.frontiersin.org

Table 1. Top 10 journals for co-citation of lipid metabolism in lung cancer.

3.3 Analysis of countries, institutions and authors

Figure 2A highlighted the collaborative efforts among a diverse range of countries and regions, particularly China, the United States, Italy, Germany, Canada, South Korea, Spain, Japan, and France. Furthermore, Figure 2B illustrated the institutional collaboration network, emphasizing the five most prolific Chinese institutions: the Chinese Academy of Sciences (CAS), Huazhong University of Science and Technology (HUST), Central South University (CSU), Nanjing Medical University (NJMU), and Sichuan University (SCU).

Figure 2
www.frontiersin.org

Figure 2. Analysis of countries, institutions and authors. (A) The visualization of countries. (B) The visualization of institutions. (C) The visualization of authors.

The authors’ collaboration network (Figure 2C) was mapped into six distinct clusters. In the network, each cluster represented a group of co-authors who predominantly originate from the same country or region. As illustrated in Figure 2C, most collaborative studies focused on clinical trials or cohort studies related to lipid metabolism in cancer. Notably, Professor Ana Ramirez de Molina, affiliated with the Madrid Institute for Advanced Studies on Food, is a distinguished expert in the field and has published five articles on lung cancer and lipid metabolism (13). Her research primarily centers on nutritional epigenetics in cancer. Similarly, Professor Wei Li from Chongqing University Cancer Hospital specializes in the role of energy metabolism in tumor cell death and has contributed four articles to this area (14, 15).

3.4 Analysis of cited articles

Utilizing VOSviewer, an analysis of the top ten most cited articles was presented in Table 2. Among these, three articles were published in the Journal of Experimental Medicine, while two appeared in Signal Transduction and Targeted Therapy and Cancer Research. The article with the highest citation count, authored by Xueli Bian in 2021 and titled “Lipid Metabolism and Cancer,” provides an extensive summary and discussion of the current understanding of lipid metabolism regulation in cancer cells. It also introduces various clinically employed strategies to disrupt lipid metabolism for cancer therapy (16). Meanwhile, the second most cited article, authored by Dingshan Li, presents an overview of the characteristics defining the interaction between ferroptosis and lipid metabolism, highlighting its significance in Cancer Research (17).

Table 2
www.frontiersin.org

Table 2. Top 10 highly cited articles in the field of lipid metabolism in lung cancer.

3.5 Keywords and research trends

Core keywords were selected using the traditional term frequency method (18). Subsequently, a total of 20 core keywords were classified into seven clusters, as illustrated in Figure 3A. These clusters encompass the following themes: “lung cancer,” “tumor microenvironment,” “lung-cancer,” “NSCLC,” “circulating triglycerides,” “transforming growth factor-beta (TGF-β),” and “drug resistance.” To elucidate the chronological progression of keywords, a timeline graph was utilized, resulting in the identification of six distinct natural clusters of keywords (Figure 3B). Notably, the clusters centered around ‘tumor microenvironment,’ ‘lipids,’ and ‘lipoprotein lipase’ emerged as focal points of research interest.

Figure 3
www.frontiersin.org

Figure 3. Analysis of keywords. (A) The clusters of keywords. (B) The timeline view map of keywords. (C) Burst detection of keywords. (D) Yearly occurrences of the top keywords.

Additionally, a citation burst analysis of the top 10 keywords in the field were visualized (Figure 3C). Citation burst analysis is a methodological tool that identifies periods of significant increases in the frequency of specific terms or phrases within a research area, thereby assisting researchers in pinpointing emerging trends and hotspots (19). The keyword “lung cancer” (2008–2015) received the most sustained attention. However, recent years have seen an increasing focus on keywords such as “tumor microenvironment” (2020–2021), “drug resistance” (2022–2024), and “lung adenocarcinoma” (2020–2024). This trend suggesting that future research is likely to concentrate on these emerging areas. In addition, the analysis of keywords illustrated the focus on lipid metabolism in lung cancer research. In Figure 3D, the color gradient denotes the frequency of keyword occurrence, with more intense red hues signifying higher frequencies. Consequently, the most prevalent keywords in recent years comprised of “lipid metabolism,” “lung cancer,” “expression,” “metabolism,” and “growth”. These findings suggested that these terms constitute current focal points of research and were anticipated to persist as principal areas of interest and activity within the domains of lung cancer and metabolism. Besides, we conducted a search in the original database using the terms “omics” and “machine learning” and created a keyword map and a timeline graph. The timeline graph showed that studies related to “omics” and “machine learning” have concentrated since 2020, with a primary focus on lipid metabolism (including fatty acid metabolism) and growth. Notably, “omics” appeared in the abstract but was not listed as a direct keyword (Supplementary Figure 1).

4 Discussion

This study represents the pioneering application of bibliometric analysis to investigate the relationship between lung cancer and lipid metabolism. We systematically collected and examined various bibliometric indicators, including the number of publications, contributing institutions and regions, leading authors, and frequently occurring keywords. This research offers a comprehensive overview of current research trends and advancements in the domain of lung cancer and lipid metabolism.

In accordance with global publication trends, research into the relationship between lung cancer and lipid metabolism has deepened progressively over the past decade. Lipid reprogramming is closely linked to the epidermal growth factor receptor (EGFR) signaling pathway, which plays a crucial role in cancer development and progression (2022). Understanding these mechanisms has unveiled potential therapeutic strategies targeting lipid metabolism for lung cancer treatment (22). In 2019, advancements in lipidomics and metabolomics technologies led to a significant surge in scholarly articles on lipid metabolism (23, 24). This demonstrates how technological innovation can drive scientific progress. Moreover, global research trends in nano-drug delivery systems for lung cancer have highlighted the importance of lipid nanoparticles as emerging hotspots (25). This may be another major reason for the increase in publications after 2019. These lipid nanoparticle systems offer promising strategies for optimizing drug delivery and overcoming drug resistance, further underscoring the critical role of lipid metabolism in lung cancer research and treatment (26).

The analysis of national and regional publication trends highlighted that China and the United States function as leading research centers across various scientific disciplines. Research institutions such as the CAS and HUST have emerged as significant contributors to lung cancer research, particularly in the context of advancements in metabolism regulation and extracellular vesicles. CAS is recognized for its prolific output and collaboration with other leading research centers globally. In the field of metabolomics, CAS has been instrumental in identifying novel recurrence-associated lipid metabolism signatures in early-stage lung adenocarcinoma (27). Specifically, the development of phospholipid phosphatase 2 (PLPP2)-mediated lipid raft synthesis represents an important biological event in the early progression of lung adenocarcinoma, providing potential targets for more precise diagnosis and treatment in clinical settings (28). Moreover, HUST has made substantial contributions to the study of extracellular vesicles in lung cancer. They conducted a metabolomic investigation of urinary extracellular vesicles for early detection and screening of lung cancer. The marker panel demonstrated effective prediction with an area under the curve (AUC) value of 84% (29).

Professor Ana Ramirez de Molina’s research focuses on the nutritional epigenetics of tumors while targeting cancer metabolism through lipid metabolism in cancer treatment and prognosis (30). This approach is supported by studies that underscore the critical role of lipid metabolism in cancer stem cells, which are well-known for their resistance to conventional therapies and their involvement in tumor recurrence (31). By integrating insights from nutritional epigenetics and cancer metabolism, her research enhances our understanding of how metabolic pathways can be modulated to improve cancer treatment outcomes.

Ferroptosis has been identified as a pivotal pathway in lung cancer, closely associated with lipid metabolism. This process is regulated by lipid metabolism, redox homeostasis, and epigenetic modifications, providing new avenues for precision therapy and overcoming drug resistance. For instance, hydrogen sulfide-induced persulfidation modulated homocysteine metabolism and potentiated ferroptosis in non-small-cell lung cancer (32). Furthermore, the combination of ferroptosis inducers with immune checkpoint inhibitors had the potential to enhance therapeutic outcomes by modulating the tumor immune microenvironment (33).

Keyword analysis revealed that lipid metabolism played a crucial role in the development of drug resistance in lung cancer (34). This association was based on the complex interaction between lipid metabolic pathways and cancer cell survival mechanisms. Alterations in lipid metabolism within cancer cells could lead to increased lipid synthesis or uptake, thereby facilitating rapid cell proliferation and contributing to drug resistance. For instance, the reprogramming of lipid metabolism has been implicated in resistance to therapies targeting the epidermal growth factor receptor (EGFR) in non-small cell lung cancer (NSCLC) (35). Additionally, modulation of lipid metabolism by drugs such as Anlotinib has been demonstrated to influence cancer cell sensitivity, suggesting that targeting lipid metabolic pathways could enhance the efficacy of existing treatments (36). Besides, lipid metabolism could also serve as a potential biomarker for diagnosing lung cancer. Tang et al. conducted the largest prospective untargeted metabolomics analysis in the Cancer Prevention Studies cohorts, identifying sphingomyelin (d18:0/22:0) and taurodeoxycholic acid 3-sulfate as metabolites positively associated with lung cancer risk, particularly stronger within three years of diagnosis. These metabolites may serve as potential screening biomarkers for lung cancer (37).

The tumor microenvironment was also highlighted in the keywords, with the interaction between lipid metabolism and immune responses playing a critical role in influencing the effectiveness of immunotherapies. Lipid metabolic reprogramming can modulate immune cell infiltration and function, thereby impacting the response to immune checkpoint inhibitors in lung cancer (38). This underscores the potential of targeting lipid metabolism not only to overcome drug resistance but also to improve the outcomes of immunotherapy (38, 39). Clinically, many anti-tumor drugs targeting lipid metabolism have emerged, and some have shown remarkable anti-tumor effects. The main issue now is enhancing the specificity of these inhibitors while maintaining normal cellular metabolism (40).

Nevertheless, this study is subject to several limitations. Primarily, the literature review was limited to sources available in the Web of Science Core Collection (WoSCC) database, which may have resulted in the omission of pertinent articles indexed in other databases. Additionally, the inclusion criteria were not exhaustive, potentially excluding relevant studies that could have enriched the analysis and provided a more comprehensive understanding of the subject matter. The reliance on a single database, such as WoSCC, inherently limits the breadth of the literature review. a more rigorous methodology would involve querying additional databases, including PubMed, Scopus, and Embase, to ensure a more comprehensive collection of relevant studies. This approach would mitigate the risk of overlooking critical studies and offer a more balanced and accurate representation of the existing body of research.

5 Conclusion

This study utilized bibliometric analysis to visualize research articles on lung cancer and lipid metabolism published between 1995 and 2024, identifying key trends, focal areas, and emerging topics. The findings indicate a notable increase in publications, with a significant contribution from China and the United States. Lipid metabolism is essential for meeting the energy and structural requirements of cancer cells, influencing signaling pathways that govern cell survival and proliferation. Additionally, it plays a pivotal role in the development of drug resistance in lung cancer.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding authors.

Author contributions

CW: Data curation, Visualization, Writing – original draft. ML: Software, Writing – original draft. WW: Resources, Validation, Writing – original draft. YJ: Data curation, Writing – review & editing. JZ: Formal analysis, Methodology, Writing – original draft. YZ: Investigation, Software, Writing – review & editing. BZ: Funding acquisition, Resources, Supervision, Writing – review & editing. WYW: Funding acquisition, Project administration, Supervision, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by the Medical and Health Science and Technology Project of Shandong Province (202311001051), Tai’an city science and technology innovation development project (2023NS407), Scientific and technological innovation plan of medical system workers in Shandong province (SDYWZGKCJHLH2023100).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2025.1562621/full#supplementary-material

References

1. Wolf AMD, Oeffinger KC, Shih TY-C, Walter LC, Church TR, Fontham ETH, et al. Screening for lung cancer: 2023 guideline update from the american cancer society. CA Cancer J Clin. (2024) 74:50–81. doi: 10.3322/caac.21811

PubMed Abstract | Crossref Full Text | Google Scholar

2. Leiter A, Veluswamy RR, Wisnivesky JP. The global burden of lung cancer: current status and future trends. Nat Rev Clin Oncol. (2023) 20:624–39. doi: 10.1038/s41571-023-00798-3

PubMed Abstract | Crossref Full Text | Google Scholar

3. Zhou J, Xu Y, Liu J, Feng L, Yu J, Chen D. Global burden of lung cancer in 2022 and projections to 2050: incidence and mortality estimates from globocan. Cancer Epidemiol. (2024) 93:102693. doi: 10.1016/j.canep.2024.102693

PubMed Abstract | Crossref Full Text | Google Scholar

4. Gu Q, Wang Y, Yi P, Cheng C. Theoretical framework and emerging challenges of lipid metabolism in cancer. Semin Cancer Biol. (2024) 108:48–70. doi: 10.1016/j.semcancer.2024.12.002

PubMed Abstract | Crossref Full Text | Google Scholar

5. Cheng C, Geng F, Cheng X, Guo D. Lipid metabolism reprogramming and its potential targets in cancer. Cancer Commun (Lond). (2018) 38:27. doi: 10.1186/s40880-018-0301-4

PubMed Abstract | Crossref Full Text | Google Scholar

6. Bai R, Meng Y, Cui J. Therapeutic strategies targeting metabolic characteristics of cancer cells. Crit Rev Oncol Hematol. (2023) 187:104037. doi: 10.1016/j.critrevonc.2023.104037

PubMed Abstract | Crossref Full Text | Google Scholar

7. Khan F, Elsori D, Verma M, Pandey S, Obaidur Rab S, Siddiqui S, et al. Unraveling the intricate relationship between lipid metabolism and oncogenic signaling pathways. Front Cell Dev Biol. (2024) 12:1399065. doi: 10.3389/fcell.2024.1399065

PubMed Abstract | Crossref Full Text | Google Scholar

8. Printz C. The cancer and metabolism link: researchers increasingly target metabolism in the search for new cancer treatments. Cancer. (2013) 119:2665–6. doi: 10.1002/cncr.28244

PubMed Abstract | Crossref Full Text | Google Scholar

9. Xu H, Wang L, Xu D. Global publication productivity and research trends on recurrent ovarian cancer: A bibliometric study. Front Oncol. (2024) 14:1422213. doi: 10.3389/fonc.2024.1422213

PubMed Abstract | Crossref Full Text | Google Scholar

10. RenChen X, Wang W, Lu Y. Emerging trends in silicosis research: A scientometric review. Environ Sci pollut Res Int. (2023) 30:113280–96. doi: 10.1007/s11356-023-30418-7

PubMed Abstract | Crossref Full Text | Google Scholar

11. Lin F, Chen Y, Mo W, Zhou H, Xiao Z, Hu S, et al. A bibliometric analysis of autophagy in lung diseases from 2012 to 2021. Front Immunol. (2022) 13:1092575. doi: 10.3389/fimmu.2022.1092575

PubMed Abstract | Crossref Full Text | Google Scholar

12. van Eck NJ, Waltman L. Software survey: vosviewer, a computer program for bibliometric mapping. Scientometrics. (2010) 84:523–38. doi: 10.1007/s11192-009-0146-3

PubMed Abstract | Crossref Full Text | Google Scholar

13. Merino Salvador M, Fernández LP, Moreno-Rubio J, Colmenarejo G, Casado E, Ramírez de Molina A, et al. Clinical features and lipid metabolism genes as potential biomarkers in advanced lung cancer. BMC Cancer. (2023) 23:36. doi: 10.1186/s12885-023-10509-x

PubMed Abstract | Crossref Full Text | Google Scholar

14. Yao X, Li W, Fang D, Xiao C, Wu X, Li M, et al. Emerging roles of energy metabolism in ferroptosis regulation of tumor cells. Adv Sci (Weinh). (2021) 8:e2100997. doi: 10.1002/advs.202100997

PubMed Abstract | Crossref Full Text | Google Scholar

15. Yang P, Qin H, Li Y, Xiao A, Zheng E, Zeng H, et al. Cd36-mediated metabolic crosstalk between tumor cells and macrophages affects liver metastasis. Nat Commun. (2022) 13:5782. doi: 10.1038/s41467-022-33349-y

PubMed Abstract | Crossref Full Text | Google Scholar

16. Bian X, Liu R, Meng Y, Xing D, Xu D, Lu Z. Lipid metabolism and cancer. J Exp Med. (2021) 218:e20201606. doi: 10.1084/jem.20201606

PubMed Abstract | Crossref Full Text | Google Scholar

17. Li D, Li Y. The interaction between ferroptosis and lipid metabolism in cancer. Signal Transduct Target Ther. (2020) 5:108. doi: 10.1038/s41392-020-00216-5

PubMed Abstract | Crossref Full Text | Google Scholar

18. Angarita-Zapata JS, Maestre-Gongora G, Calderín JF. A bibliometric analysis and benchmark of machine learning and automl in crash severity prediction: the case study of three Colombian cities. Sensors (Basel). (2021) 21:8401. doi: 10.3390/s21248401

PubMed Abstract | Crossref Full Text | Google Scholar

19. Jiang S, Liu Y, Zheng H, Zhang L, Zhao H, Sang X, et al. Evolutionary patterns and research frontiers in neoadjuvant immunotherapy: A bibliometric analysis. Int J Surg. (2023) 109:2774–83. doi: 10.1097/JS9.0000000000000492

PubMed Abstract | Crossref Full Text | Google Scholar

20. Zhao M, Yuan H, Yang G, Wang Y, Bu Y, Zhang H, et al. Tumour cell-expressed pd-L1 reprograms lipid metabolism via egfr/itgb4/srebp1c signalling in liver cancer. JHEP Rep. (2024) 6:101009. doi: 10.1016/j.jhepr.2024.101009

PubMed Abstract | Crossref Full Text | Google Scholar

21. Huang Q, Wang Q, Li D, Wei X, Jia Y, Zhang Z, et al. Co-administration of 20(S)-protopanaxatriol (G-ppt) and egfr-tki overcomes egfr-tki resistance by decreasing scd1 induced lipid accumulation in non-small cell lung cancer. J Exp Clin Cancer Res. (2019) 38:129. doi: 10.1186/s13046-019-1120-4

PubMed Abstract | Crossref Full Text | Google Scholar

22. Eltayeb K, La Monica S, Tiseo M, Alfieri R, Fumarola C. Reprogramming of lipid metabolism in lung cancer: an overview with focus on egfr-mutated non-small cell lung cancer. Cells. (2022) 11:413. doi: 10.3390/cells11030413

PubMed Abstract | Crossref Full Text | Google Scholar

23. Wang R, Li B, Lam SM, Shui G. Integration of lipidomics and metabolomics for in-depth understanding of cellular mechanism and disease progression. J Genet Genomics. (2020) 47:69–83. doi: 10.1016/j.jgg.2019.11.009

PubMed Abstract | Crossref Full Text | Google Scholar

24. Tyurina YY, Tyurin VA, Anthonymuthu T, Amoscato AA, Sparvero LJ, Nesterova AM, et al. Redox lipidomics technology: looking for a needle in a haystack. Chem Phys Lipids. (2019) 221:93–107. doi: 10.1016/j.chemphyslip.2019.03.012

PubMed Abstract | Crossref Full Text | Google Scholar

25. Zhang H, Li Y, Huang J, Shen L, Xiong Y. Precise targeting of lipid metabolism in the era of immuno-oncology and the latest advances in nano-based drug delivery systems for cancer therapy. Acta Pharm Sin B. (2024) 14:4717–37. doi: 10.1016/j.apsb.2024.07.021

PubMed Abstract | Crossref Full Text | Google Scholar

26. Yu C, Fan C-Q, Chen Y-X, Guo F, Rao H-H, Che P-Y, et al. Global research trends and emerging hotspots in nano-drug delivery systems for lung cancer: A comprehensive bibliometric analysis (1998-2024). Discovery Oncol. (2025) 16:33. doi: 10.1007/s12672-025-01782-2

PubMed Abstract | Crossref Full Text | Google Scholar

27. Zhu M, Zeng Q, Fan T, Lei Y, Wang F, Zheng S, et al. Clinical significance and immunometabolism landscapes of a novel recurrence-associated lipid metabolism signature in early-stage lung adenocarcinoma: A comprehensive analysis. Front Immunol. (2022) 13:783495. doi: 10.3389/fimmu.2022.783495

PubMed Abstract | Crossref Full Text | Google Scholar

28. Wang Y, Miao Z, Qin X, Yang Y, Wu S, Miao Q, et al. Transcriptomic landscape based on annotated clinical features reveals plpp2 involvement in lipid raft-mediated proliferation signature of early-stage lung adenocarcinoma. J Exp Clin Cancer Res. (2023) 42:315. doi: 10.1186/s13046-023-02877-w

PubMed Abstract | Crossref Full Text | Google Scholar

29. Yang Q, Luo J, Xu H, Huang L, Zhu X, Li H, et al. Metabolomic investigation of urinary extracellular vesicles for early detection and screening of lung cancer. J Nanobiotechnology. (2023) 21:153. doi: 10.1186/s12951-023-01908-0

PubMed Abstract | Crossref Full Text | Google Scholar

30. Huang X, Hou S, Li Y, Xu G, Xia N, Duan Z, et al. Targeting lipid metabolism via nanomedicine: A prospective strategy for cancer therapy. Biomaterials. (2024) 317:123022. doi: 10.1016/j.biomaterials.2024.123022

PubMed Abstract | Crossref Full Text | Google Scholar

31. Visweswaran M, Arfuso F, Warrier S, Dharmarajan A. Aberrant lipid metabolism as an emerging therapeutic strategy to target cancer stem cells. Stem Cells. (2020) 38:6–14. doi: 10.1002/stem.3101

PubMed Abstract | Crossref Full Text | Google Scholar

32. Zheng H, Chen H, Cai Y, Shen M, Li X, Han Y, et al. Hydrogen sulfide-mediated persulfidation regulates homocysteine metabolism and enhances ferroptosis in non-small cell lung cancer. Mol Cell. (2024) 84:4016–30. doi: 10.1016/j.molcel.2024.08.035

PubMed Abstract | Crossref Full Text | Google Scholar

33. Niu X, Chen L, Li Y, Hu Z, He F. Ferroptosis, necroptosis, and pyroptosis in the tumor microenvironment: perspectives for immunotherapy of sclc. Semin Cancer Biol. (2022) 86:273–85. doi: 10.1016/j.semcancer.2022.03.009

PubMed Abstract | Crossref Full Text | Google Scholar

34. Vishwa R, BharathwajChetty B, Girisa S, Aswani BS, Alqahtani MS, Abbas M, et al. Lipid metabolism and its implications in tumor cell plasticity and drug resistance: what we learned thus far? Cancer Metastasis Rev. (2024) 43:293–319. doi: 10.1007/s10555-024-10170-1

PubMed Abstract | Crossref Full Text | Google Scholar

35. Jin C, Yuan P. Implications of lipid droplets in lung cancer: associations with drug resistance. Oncol Lett. (2020) 20:2091–104. doi: 10.3892/ol.2020.11769

PubMed Abstract | Crossref Full Text | Google Scholar

36. Zhu Z, Xu S, Ren J, Jiang T, Zhang C, Yan Z. Anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells. Lipids Health Dis. (2023) 22:134. doi: 10.1186/s12944-023-01907-y

PubMed Abstract | Crossref Full Text | Google Scholar

37. Tang Z, Liang D, Deubler EL, Sarnat JA, Chow SS, Diver WR, et al. Lung cancer metabolomics: A pooled analysis in the cancer prevention studies. BMC Med. (2024) 22:262. doi: 10.1186/s12916-024-03473-1

PubMed Abstract | Crossref Full Text | Google Scholar

38. Cheng T, Zhang J, Liu D, Lai G, Wen X. Prognosis of non-small-cell lung cancer patients with lipid metabolism pathway alternations to immunotherapy. Front Genet. (2021) 12:646362. doi: 10.3389/fgene.2021.646362

PubMed Abstract | Crossref Full Text | Google Scholar

39. Bacci M, Lorito N, Smiriglia A, Morandi A. Fat and furious: lipid metabolism in antitumoral therapy response and resistance. Trends Cancer. (2021) 7:198–213. doi: 10.1016/j.trecan.2020.10.004

PubMed Abstract | Crossref Full Text | Google Scholar

40. Liang K, Dai J-Y. Progress of potential drugs targeted in lipid metabolism research. Front Pharmacol. (2022) 13:1067652. doi: 10.3389/fphar.2022.1067652

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: lipid metabolism, lung cancer, bibliometric, visualized analysis, trend

Citation: Wang C, Lei M, Wang W, Jiang Y, Zhang J, Zhang Y, Zhao B and Wang W (2025) The rising influence of lipid metabolism in lung cancer: a global research perspective. Front. Oncol. 15:1562621. doi: 10.3389/fonc.2025.1562621

Received: 17 January 2025; Accepted: 04 March 2025;
Published: 31 March 2025.

Edited by:

Dong Hu, Anhui University of Science and Technology, China

Reviewed by:

Xin Zhang, Shandong University, China
Qing Li, Anhui Provincial Hospital, China

Copyright © 2025 Wang, Lei, Wang, Jiang, Zhang, Zhang, Zhao and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Wenyang Wang, d2VueWFuZzExQHNpbmEuY29t; Bin Zhao, emhhb2JpbjAyMjBAMTYzLmNvbQ==

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Research integrity at Frontiers

Man ultramarathon runner in the mountains he trains at sunset

95% of researchers rate our articles as excellent or good

Learn more about the work of our research integrity team to safeguard the quality of each article we publish.


Find out more