Bo Li1
Zhuo Liu- 1Department of Rehabilitation Medicine, China-Japan Union Hospital of Jilin University, Changchun, China
- 2Department of Education, Jilin University Second Hospital, Changchun, China
- 3Department of Gastrointestinal Colorectal and Anal Surgery, China-Japan Union Hospital of Jilin University, Changchun, China
Colorectal cancer (CRC) is a worldwide disease threatening people's lives. Surgery and chemotherapy are still the main methods for CRC treatment. However, the side effects and chemotherapeutic drug resistance restrict the application of chemotherapy. Trametes Robiniophila Murr, also known as Huaier, is a traditional Chinese medicine that has been used for more than 1,600 years. Huaier extracts have promising anti-cancer effects on hepatoma, breast cancer, and gastric cancer. Nowadays, the tumor inhibition of Huaier on CRC has attracted more and more attention. This review mainly provides the possible anti-tumor mechanisms of Huaier for CRC treatment in apoptosis and inhibiting proliferation of tumor cells, preventing epithelial-mesenchymal transformation (EMT), weakening proliferation and differentiation of CRC stem cells, decreasing the vessel density in tumor tissues, and enhancing the immune system and chemotherapeutic efficacy. Huaier extract may be a good candidate for CRC treatment, especially when combined with other chemotherapeutic agents.
Introduction
Colorectal cancer (CRC) is a common malignant tumor in the digestive tract, and its incidence is increasing. The mortality of CRC is on the rise and ranks third among all malignancies (1) that seriously endanger the health of people. Surgery is still the most important current treatment method for CRC, but the average 5-year survival rate is < 50%, and about 30% of patients may develop tumor recurrence after surgery (2). Chemotherapy and radiotherapy are still the most commonly used methods to prevent the post-surgical tumor recurrence or treat the advanced CRC that is unsuitable for surgical resection. However, the side effects of chemotherapy and radiotherapy cannot be restricted nowadays. Therefore, developing new anti-cancer drugs with low toxicity and drug resistance is urgent. More and more researchers are focusing on the effects of Chinese medicine in postoperative adjuvant therapy for many years. Post-surgical adjuvant therapy by Chinese medicine can effectively enhance the effect of chemotherapy, reduce the toxic side effects of chemotherapy and adverse reactions caused by surgery, etc., and improve the survival rate and the quality of life of CRC patients (3, 4).
Trametes Robiniophila Murr, also known as Huaier, has a history of more than 1,600 years as traditional Chinese medicine. Huaier granules are common clinical pharmaceutical agents. Huaier is a medicinal fungus that grows on acacia, locust tree, sandalwood and many other trees, and it contains various organic components and more than 10 minerals. The main ingredient of Huaier is the fungal matter, which includes polysaccharides, proteins, ketones, and alkaloids, and the active ingredient is polysaccharide-protein (5). Huaier granules have shown promising tumor inhibitory effects on many kinds of cancers, including hepatic cancer (6), breast cancer (7), and gastric cancer (8). It is reported that Huaier extracts can effectively inhibit the proliferation of colon cancer cells (9) and prevent the progression of colon tumors in nude mice (10). These findings may provide new aspects for CRC treatment. However, the concrete mechanisms of Huaier against CRC are not clear. As a result, this review mainly provides the possible anti-tumor mechanisms of Huaier for CRC treatment (Figure 1).
Figure 1. Mechanisms of Trametes Robiniophila Murr for CRC treatment.
The role of Huaier in CRC cells
Promoting apoptosis and inhibiting proliferation of tumor cells
Huaier can inhibit the proliferation of CRC cells by inducing tumor apoptosis. It is reported that Huaier extract can induce G0/G1 and S phrases arrest, and the proliferation ability of tumor cells is weakened and the ability of apoptosis is enhanced (11, 12). Studies have shown that wild-type p53 protein encoded by the p53 gene inhibits cell growth, induces apoptosis, and repairs damaged cells. These functions are related to genomic stability, cell cycle progression, apoptosis, and DNA damage repair (13). Bcl-2 can regulate tumor cell apoptosis and inhibit cancer cell proliferation through the mitochondrial pathway (14). Lin et al. found that Huaier extract can improve the severity of inflammatory bowel disease-related tumors, induce apoptosis of related tumor cells, and inhibit tumor cell proliferation in CRC mouse model. In addition, the apoptosis-associated protein levels, including p53 and Bcl-2, show significant differences when treated with Huaier in CRC cell lines (15). Therefore, Huaier may possess good properties to induce apoptosis of CRC cells by activating and upregulating p53 and downregulating Bcl-2/Bax genes. Sun et al. have reported that Huaier granules can significantly decrease the tumor development in nude mice transplanted with HT-29 colon carcinoma cell line by downregulating the expression of PI3KR1, Akt, Wnt1, CTTNB1, and Notch genes (9). It is reported that chromosomal maintenance protein is a target for Huaier in hepatocellular carcinoma, and Huaier inhibits the cell cycle of liver cancer cells by regulating chromosomal maintenance proteins, thereby inhibiting tumors (11). In addition, Huaier extracts can inhibit proliferation and induction of apoptosis in two tuberous sclerosis complex cell models by inhibiting JAK2/STAT3 and MAPK signaling pathways (16). However, the above mechanisms of Huaier should be further investigated in CRC cell lines or animal models.
Inhibiting epithelial-mesenchymal transformation
Epithelial-mesenchymal transformation (EMT) refers to the biological process by which epithelial cells are transformed into cells with interstitial phenotypes through specific procedures (17). EMT is always associated with tumor invasion and distant metastasis (18). Matrix metalloproteinase (MMP) plays an essential role in the EMT by influencing the degradation and remodeling of the extracellular matrix, increasing local invasion of tumor cells, and improving distant metastasis (19). Researchers found that Huaier can decrease the expressions of Bcl-2, MMP-2, and MMP-9 in the MKN-45 cell line, thus inducing apoptosis and preventing the invasion of tumor cells (20). Huaier may reduce the invasion and metastasis of CRC cells by inhibiting EMT. The effects may be associated with the regulation of the expression of messenger RNA and the transcription factors. Furthermore, Huaier extracts can slow the growth of pancreatic cancer and decrease the invasion, migration, and EMT of pancreatic cancer cells by suppressing Wnt/beta-catenin pathway (21). However, the inhibitory effect of Huaier on EMT in CRC treatment remains to be further studied.
The role of Huaier in CRC stem cells
CRC stem cells have a stronger ability to proliferate, infiltrate, and metastasize than CRC cells (22). Inhibiting the proliferation, invasion, and migration of tumor stem cells can decrease the proportion of stem cells transformed into cancer cells, thus preventing the recurrence and migration of tumors (23). The proliferation, differentiation, and self-renew ability of CRC stem cells are regulated by multiple signaling pathways. The expression of messenger RNA associated with tumor proliferation in CRC stem cells treated with Huaier granules is significantly downregulated, and the proliferation of stem cells is inhibited (9). Huaier extracts inhibit the migration of CRC and may be achieved by down-regulating the expression of messenger RNA of key genes or proteins to attenuate the properties of cancer stem cells. Detailed mechanisms about the effect of Huaier on CRC stem cells need to be further verified.
The role of Huaier in tumor angiogenesis
Neovascularization is a typical feature of tumors and is a necessary process for tumor invasion and distant metastasis (24, 25). Neogenesis in tumors is regulated by various angiogenesis factors, such as vascular endothelial growth factor (VEGF) and its regulatory gene hypoxia inducing factor 1α, human macrophage metal elastase (26, 27). The overexpression of VEGF is strongly associated with poor treatment outcomes and reduced survival rates in cancer patients (28, 29). Therefore, inhibiting the proliferation of vascular endothelial cells induced by VEGF is the key to preventing tumor invasion and migration. Zheng et al. found that Huaier polysaccharide (TP-1) can reduce the expression of hypoxia-inducible factor and VEGF in tumor tissues in mice bearing hepatocellular carcinoma SMMC-7721 tumors model (30). Huaier extracts can not only decrease VEGF levels in mouse mammary tumor cells but also decrease microvessel density in tumor tissues (31). Huaier granules can suppress the infiltration of tumor-associated macrophages, and inhibit the angiogenesis of macrophages, thereby inhibiting tumor progression in RAW264.7 murine macrophage cell line (32). However, this effect has not been tested in CRC.
Huaier extracts can inhibit the invasion and migration of CRC by inhibiting neovascularization in the tumor, which may be the focus of future clinical research and can be applied in the clinical treatment of CRC. However, more experiments are needed to validate and explore the possible molecular mechanisms of the effects of Huaier on tumor angiogenesis.
The role of Huaier in the immune system
The balance between tumor-specific immunity and tolerance affects the health of the host. Under the protection of the immune system, a normal organism can prevent the deterioration of mutated tumor cells. However, cellular immune function in CRC gradually decreases and continues to deteriorate with tumor progress, recurrence, and distant metastasis (33, 34). Therefore, it is of great significance to protect and enhance the immune defense ability to increase the efficacy of anti-tumor therapy for CRC patients. As a traditional Chinese medicine, Huaier extracts can act as an effective immune enhancer and modulator by fully mobilizing cellular and humoral immunity, thus reducing the cachexia caused by chemotherapy (5, 35). Huaier granules can enhance the phagocytosis of macrophages, increase the number and activity of natural killer cells, and enhance the body's immunity to effectively induce the death of tumor cells (19, 36). Huaier granules can promote the maturation of dendritic cells, and the dendritic cells treated by Huaier can significantly stimulate the proliferation of CD4+T cells and promote their differentiation into the Th1 subgroup (37). In one study, the researchers found that Huaier polysaccharides can decrease the nephrotoxicity caused by cisplatin chemotherapy and protect renal function by regulating PI3K/Akt/mTOR signaling pathway in vitro, thus enhancing the immune ability of patients (38). Huaier extracts can perform the anti-tumor effects by enhancing the immune system, but detailed mechanisms still need further study.
Enhancing chemotherapeutic efficacy
Clinically, the main causes of tumor deaths are metastasis and recurrence (39, 40). Tumor metastasis is a multistep process in which tumor cells penetrate stromal tissue, blood, or lymph node metastasis, adhere to the basement membrane, and invade the target organ (41, 42). Although chemotherapy, radiotherapy, and targeted therapy can decrease the recurrence and metastasis of cancer, there are still some problems that need to be solved, such as insensitivity to chemotherapy drugs and drug resistance. Chemotherapy still plays a dominant role in the comprehensive treatment of CRC, so it is significant to enhance chemotherapy sensitivity. The inhibition of EMT can increase the chemotherapy sensitivity of CRC to oxaliplatin (43). It is reported that Huaier extracts can prevent EMT (21), which may be used to increase chemotherapy sensitivity. Studies have shown that Huaier plays an effect on the reversal of chemotherapeutic agents resistance, thus increasing the chemotherapy effects (44, 45). The efficacy of Huaier combined with paclitaxel in treating BT474 and MDA-MB-231 breast cancer-bearing mice is superior to that of paclitaxel alone. The combination of Huaier and paclitaxel can reduce the levels of PI3K and p-AKT (46). In one meta-analysis, the researchers concluded that Huaier granules can enhance the chemotherapeutic efficacy of gastric cancer (8). Huaier granules can increase the sensitivity of chemotherapy and inhibit the recurrence and metastasis of tumors. However, a large number of basic and clinical studies need to confirm its effect on CRC and its specific mechanism.
Conclusions and perspectives
There are still some problems that need to be solved to be widely applied in CRC treatment. (1) The active ingredient of Huaier for tumor treatment has not been determined. (2) Although increasing studies have focused on the direct effects of Huaier on cancer cells, few studies have explored its molecular and immunomodulatory mechanisms. (3) Whether the inhibitory effect of Huaier granules on the invasion and migration of CRC is related to the influence of intestinal flora needs further study. (4) More basic and clinical studies should be performed to provide a more convincing basis for applying Huaier in the treatment of CRC.
In conclusion, Huaier extracts may inhibit the progression of CRC in various ways, include inducing apoptosis and inhibition of tumor cell proliferation, blocking epithelial mesenchymal transition (EMT), attenuating proliferation and differentiation of CRC stem cells, reducing vascular density in tumor tissue, and enhancing the immune system. Therefore, Huaier may be an excellent candidate to enhance the sensitivity of chemotherapy while enhancing the immune system and decreasing side effects. The genes, signaling pathways, and related molecular mechanisms involved in the interaction between Huaier extracts and CRC are the focuses of future research.
Author Contributions
BL drafted the review. QC generated the graph and guided the construction of the manuscript. ZL edited the review. All authors contributed to the article and approved the submitted version.
Funding
This study was supported by Science and Technology Department of Jilin Province (20200201325JC).
Acknowledgments
We also thank Qidong Gaitianli Pharmaceutical Co. LTD for providing theoretical and financial support.
Conflict of interest
The authors declare that this study received funding from Qidong Gaitianli Pharmaceutical Co., LTD. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
Publisher's note
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References
1. Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer statistics, 2022. CA Cancer J Clin. (2022) 72:7–33. doi: 10.3322/caac.21708
2. Labianca R, Nordlinger B, Beretta GD, Mosconi S, Mandala M, Cervantes A, et al. Early colon cancer: esmo clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. (2013) 24:64–72. doi: 10.1093/annonc/mdt354
3. Guo T-h, Li Y-y, Hong S-w, Cao Q-y, Chen H, Xu Y, et al. Evidence for anticancer effects of chinese medicine monomers on colorectal cancer. Chin J Integr Med. (2022). doi: 10.1007/s11655-022-3466-2. [Epub ahead of print].
4. Jiang H-Z, Jiang Y-L, Yang B, Long F-X, Yang Z, Tang D-X. Traditional chinese medicines and capecitabine-based chemotherapy for colorectal cancer treatment: a meta-analysis. Cancer Med. (2022). doi: 10.1002/cam4.4896. [Epub ahead of print].
5. Pan J, Yang C, Jiang Z, Huang J. Trametes robiniophila murr: a traditional chinese medicine with potent anti-tumor effects. Cancer Manag Res. (2019) 11:1541–9. doi: 10.2147/CMAR.S193174
6. Wang Z, Yu X-l, Zhang J, Cheng Z-g, Han Z-y, Liu F-y, et al. Huaier granule prevents the recurrence of early-stage hepatocellular carcinoma after thermal ablation: a cohort study. J Ethnopharmacol. (2021) 281:114539. doi: 10.1016/j.jep.2021.114539
7. Li C, Wang X, Chen T, Wang W, Yang Q. trametes robiniophila murr in the treatment of breast cancer. Biomed Pharmacother. (2020) 128:110254. doi: 10.1016/j.biopha.2020.110254
8. Hou D, Xiong J, Yang L, Xiong L. Efficacy and safety of huaier granules combined with chemotherapy for gastric cancer a protocol for systematic review and meta-analysis. Medicine. (2020) 99:e21807. doi: 10.1097/MD.0000000000021807
9. Sun W-W, Dou J-X, Zhang L, Qiao L-K, Shen N, Zhao Q, et al. Killing effects of huaier granule combined with Dc-Cik on nude mice transplanted with colon carcinoma cell line. Oncotarget. (2017) 8:46081–9. doi: 10.18632/oncotarget.17687
10. Sun W-W, Dou J-X, Zhang L, Qiao L-K, Shen N, Gao W-Y. Killing effect of huaier combined with dc-cik on nude mice bearing colon cancer ht29 stem cells in vivo. Zhongguo Zhong Yao Za Zhi. (2018) 43:168–73. doi: 10.19540/j.cnki.cjcmm.20161222.055
11. Niu Y, Shan L, Gao H, Zhang C, Qian Z, Wang Z, et al. Huaier suppresses the hepatocellular carcinoma cell cycle by regulating minichromosome maintenance proteins. Onco Targets Ther. (2020) 13:12015–25. doi: 10.2147/OTT.S279723
12. Xu D-q, Yuan X-j, Toyoda H, Hirayama M. Anti-tumor effect of huaier extract against neuroblastoma cells in vitro. Int J Med Sci. (2021) 18:1015–23. doi: 10.7150/ijms.48219
13. Borrero LJH, El-Deiry WS. Tumor suppressor P53: biology, signaling pathways, and therapeutic targeting. Biochim Biophys Acta Rev Cancer. (2021) 1876:188556. doi: 10.1016/j.bbcan.2021.188556
14. Adams JM, Cory S. The Bcl-2 arbiters of apoptosis and their growing role as cancer targets. Cell Death Differ. (2018) 25:27–36. doi: 10.1038/cdd.2017.161
15. Zou Y-f, Rong Y-m, Chen Z-x, Shen Z-h, Chen X, Tan Y-x, et al. Effects of huaier extract on ameliorating colitis-associated colorectal tumorigenesis in mice. Oncotargets Ther. (2020) 13:8691–704. doi: 10.2147/OTT.S253598
16. Yang A, Fan H, Zhao Y, Zha X, Zhang H, Hu Z, et al. Huaier aqueous extract inhibits proliferation and metastasis of tuberous sclerosis complex cell models through downregulation of Jak2/Stat3 and Mapk signaling pathways. Oncol Rep. (2016) 36:1491–8. doi: 10.3892/or.2016.4969
17. Scheau C, Badarau IA, Costache R, Caruntu C, Mihai GL, Didilescu AC, et al. The role of matrix metalloproteinases in the epithelial-mesenchymal transition of hepatocellular carcinoma. Anal Cell Pathol. (2019) 2019:9423907. doi: 10.1155/2019/9423907
18. Chen T, You Y, Jiang H, Wang ZZ. Epithelial-mesenchymal transition (Emt): a biological process in the development, stem cell differentiation, and tumorigenesis. J Cell Physiol. (2017) 232:3261–72. doi: 10.1002/jcp.25797
19. Zheng J, Li C, Wu X, Liu M, Sun X, Yang Y, et al. Astrocyte elevated gene-1 (Aeg-1) shrna sensitizes huaier polysaccharide (Hp)-induced anti-metastatic potency via inactivating downstream P13k/Akt pathway as well as augmenting cell-mediated immune response. Tumor Biology. (2014) 35:4219–24. doi: 10.1007/s13277-013-1552-y
20. Ji X, Pan C, Li X, Gao Y, Xia L, Quan X, et al. Trametes robiniophila may induce apoptosis and inhibit mmps expression in the human gastric carcinoma cell line Mkn-45. Oncol Lett. (2017) 13:841–6. doi: 10.3892/ol.2016.5517
21. Zhou C, Li J, Qian W, Yue Y, Xiao Y, Qin T, et al. Huaier extract restrains pancreatic cancer by suppressing Wnt/Beta-catenin pathway. Biomed Pharmacother. (2020) 127:110126. doi: 10.1016/j.biopha.2020.110126
22. Prager BC, Xie Q, Bao S, Rich JN. Cancer stem cells: the architects of the tumor ecosystem. Cell Stem Cell. (2019) 24:41–53. doi: 10.1016/j.stem.2018.12.009
23. Ishiguro T, Ohata H, Sato A, Yamawaki K, Enomoto T, Okamoto K. Tumor-derived spheroids: relevance to cancer stem cells and clinical applications. Cancer Sci. (2017) 108:283–9. doi: 10.1111/cas.13155
24. Shanmugam MK, Warrier S, Kumar AP, Sethi G, Arfuso F. Potential role of natural compounds as anti-angiogenic agents in cancer. Curr Vasc Pharmacol. (2017) 15:503–19. doi: 10.2174/1570161115666170713094319
25. Jiang X, Wang J, Deng X, Xiong F, Zhang S, Gong Z, et al. The role of microenvironment in tumor angiogenesis. J Exp Clin Cancer Res. (2020) 39:204. doi: 10.1186/s13046-020-01709-5
26. Bielenberg DR, Zetter BR. The contribution of angiogenesis to the process of metastasis. Cancer J. (2015) 21:267–73. doi: 10.1097/PPO.0000000000000138
27. Viallard C, Larrivee B. Tumor angiogenesis and vascular normalization: alternative therapeutic targets. Angiogenesis. (2017) 20:409–26. doi: 10.1007/s10456-017-9562-9
28. Goel HL, Mercurio AM. Vegf targets the tumour cell. Nat Rev Cancer. (2013) 13:871–82. doi: 10.1038/nrc3627
29. Kloepper J, Riedemann L, Amoozgar Z, Seano G, Susek K, Yu V, et al. Ang-2/Vegf bispecific antibody reprograms macrophages and resident microglia to anti-tumor phenotype and prolongs glioblastoma survival. Proc Natl Acad Sci U S A. (2016) 113:4476–81. doi: 10.1073/pnas.1525360113
30. Li C, Wu X, Zhang H, Yang G, Hao M, Sheng S, et al. A huaier polysaccharide restrains hepatocellular carcinoma growth and metastasis by suppression angiogenesis. Int J Biol Macromol. (2015) 75:115–20. doi: 10.1016/j.ijbiomac.2015.01.016
31. Wang X, Zhang N, Huo Q, Yang Q. Anti-angiogenic and antitumor activities of huaier aqueous extract. Oncol Rep. (2012) 28:1167–75. doi: 10.3892/or.2012.1961
32. Li Y, Qi W, Song X, Lv S, Zhang H, Yang Q. Huaier extract suppresses breast cancer via regulating tumor-associated macrophages. Sci. Rep. (2016) 6:20049. doi: 10.1038/srep20049
33. Luo M, Li H, Han D, Yang K, Kang L. Inhibition of autophagy enhances apoptosis induced by ce6-photodynamic therapy in human colon cancer cells. Photodiagnosis Photodyn Ther. (2021) 36:102650. doi: 10.1016/j.pdpdt.2021.102605
34. Townsend KN, Hughson LRK, Schlie K, Poon VI, Westerback A, Lum JJ. Autophagy inhibition in cancer therapy: metabolic considerations for antitumor immunity. Immunol Rev. (2012) 249:176–94. doi: 10.1111/j.1600-065X.2012.01141.x
35. Sun Y, Sun T, Wang F, Zhang J, Li C, Chen X, et al. A polysaccharide from the fungi of huaier exhibits anti-tumor potential and immunomodulatory effects. Carbohydr Polym. (2013) 92:577–82. doi: 10.1016/j.carbpol.2012.09.006
36. Li C, Wu X, Zhang H, Yang G, Hao M, Sheng S, et al. A huaier polysaccharide inhibits hepatocellular carcinoma growth and metastasis. Tumor Biology. (2015) 36:1739–45. doi: 10.1007/s13277-014-2775-2
37. Pan J, Jiang Z, Wu D, Yang C, Wang Z, Huang J. Huaier extractum promotes dendritic cells maturation and favors them to induce Th1 immune response: one of the mechanisms underlying its anti-tumor activity. Integr Cancer Ther. (2020) 19:1534735420946830. doi: 10.1177/1534735420946830
38. Fang L, Zhang Y, Wang Q, Zang Y, Li Z, Duan Z, et al. A polysaccharide from huaier ameliorates cisplatin nephrotoxicity by decreasing oxidative stress and apoptosis via Pi3k/Akt signaling. Int J Biol Macromol. (2019) 139:932–43. doi: 10.1016/j.ijbiomac.2019.07.219
39. Tabrizian P, Jibara G, Shrager B, Schwartz M, Roayaie S. Recurrence of hepatocellular cancer after resection patterns, treatments, and prognosis. Ann Surg. (2015) 261:947–55. doi: 10.1097/SLA.0000000000000710
40. Redig AJ, McAllister SS. Breast cancer as a systemic disease: a view of metastasis. J Intern Med. (2013) 274:113–26. doi: 10.1111/joim.12084
41. Shao B, Zhao X, Liu T, Zhang Y, Sun R, Dong X, et al. Loxl2 promotes vasculogenic mimicry and tumour aggressiveness in hepatocellular carcinoma. J Cell Mol Med. (2019) 23:1363–74. doi: 10.1111/jcmm.14039
42. Grinshpun A, Ben-Porath I, Peretz T, Salmon A. Tumor, metastasis and what's in between. Harefuah. (2013) 152:30–58.
43. Guo C, Ma J, Deng G, Qu Y, Yin L, Li Y, et al. Zeb1 promotes oxaliplatin resistance through the induction of epithelial-mesenchymal transition in colon cancer cells. J Cancer. (2017) 8:3555–66. doi: 10.7150/jca.20952
44. Fu Z, Ma K, Dong B, Zhao C, Che C, Dong C, et al. The synergistic antitumor effect of huaier combined with 5-florouracil in human cholangiocarcinoma cells. BMC Complement Altern Med. (2019) 19:203. doi: 10.1186/s12906-019-2614-5
45. Qi T, Dong Y, Gao Z, Xu J. Research progress on the anti-cancer molecular mechanisms of huaier. Onco Targets Ther. (2020) 13:12587–99. doi: 10.2147/OTT.S281328
Keywords: colorectal cancer, Trametes Robiniophila Murr, Huaier, mechanisms, anticancer
Citation: Li B, Cao Q and Liu Z (2022) The treatment effects of Trametes Robiniophila Murr against colorectal cancer: A mini-review. Front. Med. 9:981516. doi: 10.3389/fmed.2022.981516
Received: 29 June 2022; Accepted: 13 July 2022;
Published: 03 August 2022.
Edited by:
Xingzhe Ma, Fresh Wind Biotechnologies, United StatesReviewed by:
Mao Lin, Fuda Cancer Hospital, ChinaYulin Dai, Changchun University of Chinese Medicine, China
Copyright © 2022 Li, Cao and Liu. 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: Zhuo Liu, emxpdSYjeDAwMDQwO2psdS5lZHUuY24=