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ORIGINAL RESEARCH article

Front. Phys., 04 July 2024
Sec. Mathematical Physics

An efficient approximate analytical technique for the fractional model describing the solid tumor invasion

  • 1Department of Mathematics, Davangere University, Davangere, India
  • 2Department of Mathematics, Zarqa University, Zarqa, Jordan
  • 3Department of Mathematics, Jain College of Engineering and Research, Belagavi, India
  • 4Department of Mathematics, Tunga Mahavidyalaya, Thirthahalli, India
  • 5Department of Mathematics, University of Mumbai, Mumbai, India

In this manuscript, we derive and examine the analytical solution for the solid tumor invasion model of fractional order. The main aim of this work is to formulate a solid tumor invasion model using the Caputo fractional operator. Here, the model involves a system of four equations, which are solved using an approximate analytical method. We used the fixed-point theorem to describe the uniqueness and existence of the model’s system of solutions and graphs to explain the results we achieved using this approach. The technique used in this manuscript is more efficient for studying the behavior of this model, and the results are accurate and converge swiftly. The current study reveals that the investigated model is time-dependent, which can be explored using the fractional-order calculus concept.

1 Introduction

After the evolution of Homo sapiens (human beings), humans are still suffering from many diseases. Among those, cancer affects the population most significantly, ranking as the second most common cause of death after cardiovascular disease. Nearly 10 million deaths have occurred, according to a 2020 survey [1]. The first cancer tumor was discovered around 3000 BCE in Egyptian mummies. Malignant tumors and neoplasms are generally called cancer [2]. The process of scattering and creating secondary tumors is known as metastasis, and this behavior of cancer cells is the key reason for death in cancer patients. However, the cause of cancer was discovered by a British surgeon Percivall Pott in 1775. The estimation of the size, phase, and growth of a tumor is very critical for the treatment of cancer, and mathematics plays an important role in helping us investigate the behavior of the tumor. Many researchers have been studying the growth of solid tumors using mathematical models [3, 4]. Discrete models that consider single cells have been constructed on them. Jeon et al., invented the discrete-continuum model [5], which gives the idea of transporting chemicals inside the tumor and the individual character of cells. Solid tumors depend on diffusion because it is the only way to intake nutrients and detach waste products. One single normal cell is converted into a main solid tumor (e.g., carcinoma [6]) due to mutations in key genes. A single tumor cell has the potential to form a group of tumor cells through successive divisions, and they develop in two different stages: one is the vascular stage, and another is the avascular stage. Then, it will cause the formation of an avascular tumor with 106 cells. Once solid tumors develop, they find a way to spread to other body parts through the circulatory system, leading to the destruction of normal tissues, and once a tumor reaches its maximum size, the absorption of nutrients is insufficient to provide the tumor’s inner parts with oxygen, which causes cell death. There are many experimental ways to model tumor cell migration, like macro-scale models and micro-patterned models [7, 8]. These solid tumors are formed due to the production of abnormal cells in the body. Another reason for the formation of solid tumors is the non-replication of DNA at the molecular level in the cell nucleus. As much research has been done and developed, many anti-cancer therapies, like radiation therapy, chemotherapy, and hormone therapy and surgery, have been implemented to increase lifespan and reduce tumors. These traditional cancer treatments do not cure it completely but involve other side effects like fatigue, vomiting, hair loss, and a reduction in blood count. However, there is a therapy called virotherapy [9], where several viruses have been used as agents to treat cancer cells, and clinical trials proved zero percent toxicity. In recent years, many mathematical models of solid tumor growth [1013] have been established, and they have also concentrated on the evolutionary dynamics of tumor growth. In this article, we will examine the solid tumor invasion model [14] of fractional order, and this model is expressed as a system of partial differential equations. The interactions between the cancer cells are denoted by Td, matrix-degrading enzymes (MDEs) are represented by Mc, the extracellular matrix is signified by Ec, and the rate of oxygen production is given by Oc. Regarding the extracellular matrix, the majority of the macromolecules are necessary for adhesion, spreading, and motility of cells. Moreover, several macromolecules, including collagen, laminin, and fibronectin, are linked to the extracellular matrix. Matrix-degrading enzymes are essential for different phases of invasion, metastasis, and turnover growth. Tumor cells produce matrix-degrading enzymes that cause the extracellular matrix to break down locally. Additionally, the way they interact with growth factors, inhibitors, and tumor cells is very complex. Here, Td and Mc and Ec and Oc have a direct linear relationship.

Fractional calculus (FC) is a tool to study derivatives and integrals of fractional order. As we know, classical calculus has been developed as a vast subject, and many researchers have been working on it until now. Due to the ideas of German mathematician Leibniz and L’Hospital’s rule, the theory of fractional calculus came into existence approximately 300 years ago. Fractional calculus can be assumed to be a well-developed and established subject. Both memory effects and hereditary properties influence the problem under consideration. FC has attracted many researchers to work on it. Compared to classical calculus, fractional calculus has more applications in various fields and real-world problems, as it gives solutions in between the intervals [15]. We all know that classical differential equations have numerous applications that model many natural and physical phenomena, but fractional differential equations (FDEs) model natural and physical phenomena more accurately, as the behaviors of FDEs give an accurate and approximate solution to the problem, which can be analyzed more understandably. Fractional-order derivatives have a greater ability to model complicated non-linear processes [1619] and higher-order behaviors. The main reason to consider fractional derivatives is that we can take any order of derivative rather than restricting it to integer order. FC has a wide variety of applications in the fields of science [20], biology [21, 22], engineering [23], and others. It allows us to study many physical phenomena, like earthquake vibrations, elasticity, shallow water waves, and quantum mechanics [2427]. Many researchers have defined fractional derivatives like Riemann–Liouville, Caputo derivative, Grünwald–Letnikov, and Atangana–Baleanu, but each operator has its own limitations. The linear and non-linear FDEs can be solved using the variational iteration method [28, 29], differential transform method [30, 31], q-homotopy analysis transform method [32], residual power series method [33], homotopy perturbation method [34, 35], and many analytical, numerical, and other techniques [3641, 57] which give analytical, numerical, and exact solutions. Recently, [42] investigated giving up smoking models with non-singular derivatives. [43] proposed the cancer-immune system model of fractional order using Caputo and Caputo–Fabrizio derivatives. [44] demonstrated the behavior of the cancer cells after injecting a dose of medicine by developing a new cancer model. [45] developed a new cancer mathematical model of fractional order using IL-10 cytokine and anti-PD-L1 inhibitors. [4648] implemented the similarity method to study multi-term time-fractional diffusion equations, Riesz fractional partial differential equations, and fractional heat equations and also deduced two variable fractional partial differential equations from ordinary differential equations. Many biological, epidemical, and other mathematical models have been studied [4956]. Here, we will apply an efficient technique called the approximate analytical method (AAM) to study the considered model. AAM is a semi-analytical method that can be used to solve highly non-linear problems, as it gives a series solution, allowing us to analyze the solution more effectively. The significance of this method is that it discretizes the non-linear terms in the equations. AAM can be applied to solve complex non-linear and linear fractional differential equations and requires less computational work. AAM has been applied to solve solute problems, fluid flow models, and KDV equations [57, 58].

2 Preliminaries

The following definitions and properties, which are utilized in this article, are cited in [17, 18, 50].

Definition 2.1: The fractional integral of a function ftCμμ1 of non-zero positive order α is defined by Riemann–Liouville (RL) and represented by

Jtα0ft=1Γα0ttϑα1fϑdϑ,J0ft=ft.

Theorem 2.2: Let b>1 and α1,α2R,α1,α20. Then, the RL fractional partial integral operator Jtα0 satisfies the following properties for the function ux,tCμ,μ>1:

Jtα10Jtα20ux,y,t=Jtα1+α20ux,y,t,Jtα10Jtα20ux,y,t=Jtα20Jtα10ux,y,t,Jtα0tb=Γb+1Γb+α+1tα+b.

Definition 2.3. The fractional derivative of fC1n in the Caputo sense is defined as

Dtαft=dnftdtn,α=nN,1Γnα0ttϑnα1fnϑdϑ,αn1,n,nN.

Definition 2.4. The Laplace transform (LT) of a Caputo fractional derivative Dtαft is denoted as

LDtαft=sαFsr=0n1sαr1fr0+,n1<αn,

where Fs denotes the LT of the function f(t).

Theorem 2.5: Let α,tR,t0,n1<α<nN. Then, we have

DtαJtα0ux,y,t=ux,y,t,Jtα0Dtα0ux,y,t=ux,y,tk=0m1tkk!kux,y,0+tk.

3 Mathematical model of solid tumor invasion

3.1 Classical model

Let us consider the classical model of solid tumor invasion, which involves a system of partial differential equations: Mc indicates the matrix-degrading enzyme (MDE) concentration, Td indicates the tumor cell density, Oc indicates the oxygen concentration, Ec indicates the concentration of macromolecules (MMs) in the extracellular matrix (EC). The values of all four variables depend on both x and time ζ. The motion of the tumor cells is determined by [14]

Tdζ=dn2TdρTdEc.

The value of the arbitrary motility coefficient that remains constant is denoted by dn, while the haptotatic coefficient is represented by ρ > 0. The breakdown of the ECM occurs due to MDEs). This leads to a process of deterioration, which is given by

Ecζ=δMcEc,

where δ is a positive constant. It is believed that active MDEs are generated by tumor cells, dispersed throughout the tissue, and undergo a certain level of decomposition. The definition for the concentration of MDE is as follows:

Mcζ=dm2Mc+μTdλMc,

where the positive constants are represented as λ, dm,and μ. The diffusion coefficient of MDEs is denoted by dm.

Solid tumor needs oxygen for growth and invasion. Oxygen gets distributed among the macromolecules, undergoes decay, and is eventually absorbed by the tumor. The density of MM is directly related to the manufacture of oxygen. It is specified by

Ocζ=dc2Oc+βEcγMcαOc,

where the rate of production is given by β, the diffusion coefficient of oxygen is denoted by dc, the rate of decay is given by α, the rate of uptake is given by γ, and all other variables remain constant.

The system of equations is given by

Tdζ=dn2TdρTdEc,Ecζ=δMcEc,Mcζ=dm2Mc+μTdλMc,Ocζ=dc2Oc+βEcγMcαOc.

The adhesion between cells and the extracellular matrix is framed by the outgrowth of cells in the cell equation, represented by χ. The system is designed to operate within a square spatial domain Ω, which represents tissue. It includes specific initial conditions for every variable. It is believed that the variables stay within the tissue area under consideration. As a result, boundary ∂Ω is subjected to no-flux boundary conditions.

We can achieve dimensionless equations by implementing non-dimensionalization through appropriate parameters such as length scale L and time τ. This approach helps simplify the equations and makes them easier to analyze; we scale the parameters as follows: the density of the tumor cell as Td0, the density of the ECM as Ec0, the concentration of the MDE as Mc0, and the concentration of oxygen as Oc0.

Td=TdTd0,Ec=EcEc0,Mc=McMc0,Oc=OcOc0,x=xL,ζ=ζL.

Now, the equations are given by

Tdζ=Dn2TdχTdEc,Ecζ=ηMcEc,Mcζ=Dm2Mc+kTdσMc,Ocζ=Dc2Oc+γEcωMcϕOc.(1)

where Dm = τdnL2, Dn = dmτL2, Dc=τdcL2, ꭓ = τEc0L2, η=τMc0δ, k = τμTd0Mc0, σ=τλ, γ=τβEc0Oc0, ω=τγTd0Oc0, and ɸ=τα.

3.2 Fractional model

By using the Caputo fractional derivative, the system of equations (Eq. 1) has been converted into fractional differential equations.

Dζαt0cTd=Dn2TdχTdEc,Dζαt0cEc=ηMcEc,Dζαt0cMc=Dm2Mc+kTdσMc,DζαOc=Dc2Oc+γEcωMcϕOct0c,(2)

with the initial conditions

Td0=Tdx,0=ex2ε,Ec0=Ecx,0=10.5ex2ε,Mc0=Mcx,0=0.5ex2ε,Oc0=Ocx,0=0.5ex2ε.

4 Methodology of the approximate analytical method

In order to determine the validity of this approach, we will examine the non-linear fractional partial differential equation (NFPDE) with the following initial conditions:

Dtαux¯,y¯,t=fx¯,y¯,t+Lu¯+Nu¯,m1<α<mN,iux¯,y¯,tti=fix¯,y¯,i=0,1,2,3,.m1,(3)

where Dtα is the Caputo fractional partial derivative of order α,fx¯,y¯,t is the source term, which is an analytical function, L and N represent linear and non-linear operators, and x¯=x1,x2,,xn y¯=y1,y2,,ynRn. To attain the analytical solution of the considered model, we implemented a technique called the approximate analytical method. Computational accuracy is necessary to provide appropriate piecewise analytical solutions, making it a useful tool for solving non-linear fractional differential equations. To illustrate AAM, it is essential to analyze the subsequent outcomes. The outcomes are cited in [48, 50].

Lemma 4.1: For vx¯,y¯,t=k=0rkvx¯,y¯,t, the linear operator Lu satisfies the following property:

Lvx¯,y¯,t=Lk=0rkvx¯,y¯,t=k=0rkLvkx¯,y¯,t.

Theorem 4.2. Let vx¯,y¯,t=k=0vkx¯,y¯,t and vλx¯,y¯,t=k=0λkvkx¯,y¯,t, where λ is the non-zero parameter such that 0λ1, and subsequently, the non-linear operator Nvλ satisfies the following conditions:

Nvλ=Nk=0λkvk=n=01n!δδλnNk=0λkvkλ=0λn.

Proof: Consider the Maclaurin expansion concerning 𝜆λ, which gives

Nvλ=Nk=0λkvk=Nk=0λkvkλ=0+δδλNk=0λkvkλ=0λ+12!δ2δλ2Nk=0λkvkλ=0λ2+=k=01n!δnδλnNk=0λkvkλ=0λn=k=01n!δnδλnNk=0λkvk+k=n+1λkvkλ=0λn=k=01n!δnδλnNk=0nλkvkλ=0λn.

Definition 4.3: The polynomials Pnv0,v1,v2,vn are defined as follows:

Pnv0,v1,v2,vn=1n!δnδλnNk=0nλkvkλ=0.

Remark 4.4. Let Pn=Pnv0,v1,v2,vn, as shown in Definition 4.3. The non-linear term Nvλ can be defined in terms of Pn using Theorem 4.2 as follows:

Nvλ=n=0λnPn.

4.1 Existence theorem

The following theorem presents an approximate analytical solution for a non-linear fractional partial differential equation, with its initial solution given in Eq. 3 and obtained through the AAM.

Theorem 4.6: The functions fx¯,t and fix¯ are defined as shown in Eq. 3 and m1<α<mN.

Equation 3 gives at least one solution, which is provided by

vx¯,y¯,t=ftαx¯,y¯,t+i=0m1tii!fix¯,y¯+i=0m1Ltαvk1+pk1tα,

where pk1tα and Ltαvk1 are the Riemann–Liouville partial fractional integral of order α for Pk1 and Lvk1 with regard to t, respectively.

Proof: Consider the solution vx¯,y¯,t of Eq. 3 in the analytical form:

vx¯,y¯,t=k=0vkx¯,y¯,t.(4)

Let us consider the below expression to solve the given initial value problem shown in Eq. 3:

Dtαvλx¯,y¯,t=λfx¯,y¯,t+Lvλ+Nvλ,0λ1,(5)

with initial conditions

iux¯,y¯,tti=fix¯,y¯,i=0,1,2,3,.m1.(6)

Let us suppose that Eq. 5 has the solution in the form:

vλx¯,y¯,t=k=0λkvkx¯,y¯,t.(7)

Now, let us consider Eq. 3 with the Riemann–Liouville partial integral, and using Theorem 4.2, we have

vλx¯,y¯,t=i=0m1tii!ivλx¯,y¯,0ti+λJtα0f(x¯,y¯,t+Lvλ+Nvλ.(8)

Equation 8 can be written as below using Eq. 6:

vλx¯,y¯,t=i=0m1tii!gix¯,y¯+λftαx¯,y¯,t+JtαLvλ+JtαNvλ.(9)

By substituting Eq. 7 into Eq. 9, we obtain

k=0λkvkx¯,y¯,t=i=0m1tii!gix¯,y¯+λftαx¯,y¯,t+Jtαλk=0Lλkvk+Jtαλn=01n!nλnNk=0λkvkλ=0λn.(10)

With the help of definition 4.3 and Eq. 10, we obtain

k=0λkvkx¯,y¯,t=i=0m1tii!gix¯,y¯+λftαx¯,y¯,t+Jtαλk=0Lλkvk+Jtαλn=0pnλn.(11)

Equating the coefficients of like powers of λ in Eq. 11, we get the below terms

voi=0m1tii!gix¯,y¯,v1x¯,y¯,t=ftαx¯,y¯,t+Ltαv0+Potα,v1x¯,y¯,t=Ltαvk1+Pk1tα,k=2,3,(12)

Substituting Eq. 12 into Eq. 7 gives the solution of Eq. 3. Using Eq. 4 and 7, we obtain

vx¯,y¯,t=limλ1vλx¯,y¯,t=v0x¯,y¯,t+v1x¯,y¯,t+k=2vkx¯,y¯,t.(13)

We can see that ivx¯,y¯,0ti=limλ1ivλx¯,y¯,ttigix¯,y¯=fix¯,y¯. Replacing Eq. 12 in Eq. 13 ends the proof.

5 Existence of the solution

We will explain the solution’s existence using the concepts provided below.

Definition 5.1: Let us consider a Cauchy space X,d, which is non-empty and 0λ<1. If the mapping S:XX for every x,x¯X, then it satisfies

dSx,Sx¯λdx,x¯.

Then, S has a unique fixed point x*X. If SkkN, the sequence is given by

Sk=SSk1,kN/1S1=S.

Thus, for any x0X,Sx0kk=1k= reaches the fixed point x*.

Definition 5.2: Let mN, HRm, p,qR, and h:p,q×HR be the function of s,t for x1,x2,,xmx1*,x2*,,xm*H. Here, h satisfies the generalized Lipschitz condition: hζ,x1,x2,,xmhζ,x1*,x2*,,xm*A1x1x1*+A2x2.x2*++Amxmxm*,Aj0,j=1,2,3,m.

Specifically, h satisfies the Lipschitz condition. If ,ζ(p,q and for any x,x*G, one has

hζ,xhζ,x*Axx*,A>0.

Let us examine the following set of equations:

DζαTdx,ζ=ψ1x,ζ,Td,DζαEcx,ζ=ψ2x,ζ,Ec,DζαMcx,ζ=ψ3x,ζ,Mc,DζαOcx,ζ=ψ4x,ζ,Oc.(14)

Now using the above Eq. 14, we obtain

Tdx,ζTdx,0=IζαDn2x2TdχTdxEcx+Td2Ecx2,
Ecx,ζEcx,0=IζαηMcEc,
Mcx,ζMcx,0=IζαDp2Mcx2+kTdσMc,
Ocx,ζOcx,0=IζαDc2Ocx2+γEcωMcϕOc.

Then, by defining the fractional integral, we obtain

Tdx,ζTdx,0=1Γα0ζζvα1ψ1x,v,Tddv,Ecx,ζEcx,0=1Γα0ζζvα1ψ2x,v,Ecdv,Mcx,ζMcx,0=1Γα0ζζvα1ψ3x,v,Mcdv,Ocx,ζOcx,0=1Γα0ζζvα1ψ4x,v,Ocdv.

5.1 Convergence theorem

Let us consider a mapping H:GG, which is non-linear, with Banach space G. Let us suppose that

HuHvμiuv,u,vG.

Thus, it has a fixed point convergence to a singular point within H and

vmvpμip1μiv1v0,i=1,2,3,4.

Proof: Consider the Banach space CJ,. with the norm demarcated as

gt=maxtJgt function on J.

We need to confirm whether the sequences Tdp, Ecp, and Ocp are Cauchy sequences in CJ,..

For Tdp, consider

TdmTdp=maxtJTdmTdp,=maxtJTdm1Tdp1Jtα0Dn2Tdm1x22Tdp1x2xςdm1xEcm1x+Tdm12Ecm1x2ςdp1xEcp1xTdp12Ecp1x2maxtJTdm1Tdp1Jtα0Dn2Tdm1x22Tdp1x2xςdm1xEcm1x+Tdm12Ecm1x2ςdp1xEcp1xTdp12Ecp1x2ςvαΓ1+αdv

(by convolution theorem)

Tdm1Tdp10ςDnδ12+χδ1λ1+λ2ςvαΓ1+αTdm1dv,

and the above inequality reduced to

TdmTdpμ1Tdm1Tdp1,

where

μ1=0ςDnδ12+χδ1λ1+λ2ςvαΓ1+αdv,
δ1=ςdm1xςdp1x,δ2=2Tdm1x22Tdp1x2,
λ1=Ecm1xEcp1x,λ2=2Ecm1x22Ecp1x2.

Taking m=p+1, we obtain

Tdp+1Tdpμ1TdpTdp1μ12Tdp1Tdp2..μ1pTd1Td0.

Using triangle inequality, we have

TdpTdpTdp+1Tdp+Tdp+2Tdp+1++TdpTdm1
μ1p+μ1p1+μ1p2+μ1m1Td1Td0
μ1p1μ1mp11μ1Td1Td0,

as 0<μ1<1, so 1μ1mp1<1, and then we have

TdpTdpμ1p1μ1Td1Td0.

However, Td1Td0<.Consequently,as m,TdpTdp0 proves that Tdp is a Cauchy sequence.

Similarly, we can prove that

EcmEcpμ2p1μ2Ec1Ec0,
McmMcpμ3p1μ3Mc1Mc0,
OcmOcpμ4p1μ4Oc1Oc0,

where

μ2=0ζδmζvαΓ1+αdv,
μ3=0ζdpδ22+knMcm1Mcp1σζvαΓ1+αdv,
μ4=0ζdcδ32+γEcωMcθδ3ζvαΓ1+αdv,
δ2=Ecm1xEcp1x,δ22=2Mcm1x22Mcp1x2,δ32=2Ocm1x22Ocp1x2,δ3=Ocm1xOcp1x.

This proves the theorem.

5.2 Uniqueness theorem

The solutions obtained through AAM for Eqs 1, 2 are always unique under

0<µi<1,i=1,2,3,4.

Proof: The solution for fractional partial equations is demonstrated as follows:

vx,ζ=p=0vpx,ζ.

For i=1, assume that Td and Td* are two distinct values such that

TdTd*maxtJTdTd*,
TdTd*Jtα0Dn2Tdx22Td*x2XTdxEcx+2Ecx2Td*xEc*xTd*2Ec*x2,
TdTd*0ζDn2Tdx22Td*x2)X(TdxEcx+2Ecx2Td*xEc*xTd*2Ec*x2ζvαΓ1+αdv

(by convolution theorem),

TdTd*0ζDnδ12+Xδ1λ1+λ2ζvαΓ1+αTdTd*dv,

and the above inequality is reduced to

TdpTdp*μ5TdTd*,

where

μ5=0ζDnδ12+Xδ1λ1+λ2ζvαΓ1+αdv,δ1=TdxTd*x,δ12=2Tdx22Td*x2,λ1=EcxEc*x,λ2=2Ecx22Ec*x2.

We obtain

1μTdTd*0,
TdTd*=0,0<μ<1,
Td=Td*.

Similarly, we can prove that Ec=Ec*, Mc=Mc*, and Oc=Oc*.

6 Solution of a system of equations using the AAM

Considering Eq. 2, we obtain

DζαDn2Tdx2t0c+χTdxEcx+Td2Ecx2=0,
Dζαt0c+ηMcEc=0,
Dζαt0cDm2Mcx2kTd+σMc=0,
Dζαt0cDc2Ocx2Ecγ+ωMc+ɸOc=0.

With the initial conditions shown in Eq. 2, we obtain

Td0=Tdx,0=ex2ε,
Ec0=Ecx,0=10.5ex2ε,
Mc0=Mcx,0=0.5ex2ε,
Oc0=Ocx,0=0.5ex2ε.

The above system of equations can be re-written as given below:

Dζαt0cTdx,ζ=Dn2Tdx2TdxEcx+Td2Ecx2,DζαtncEcx,ζ=ηMcEc,Dζαt0cMcx,ζ=Dm2Mcx2kTd+σMc,Dζαt0cOcx,ζ=Dc2ocx2+EcγωMcΦOc.

Using the AAM procedure, let us assume the solution of the above system of equations in the following manner:

vx,ζ=k=0vkx,ζ.(15)

Consider the above system of equations to get an approximate solution:

Dζαt0cTdλx,ζ=λDn2Tdx2TdxEcx+Td2Ecx2,Dζαt0cEcλx,ζ=ληMcEc,Dζαt0cMcλx,ζ=λDm2Mcx2+kTdσMc,Dζαt0cOcλx,ζ=λDc2Ocx2+EcγωMcɸOc,

with the assumed initial solutions

Tdλx,ζ,0=g1x,ζ,Ecλx,ζ,0=g2x,ζ,Mcλx,ζ,0=g3x,ζ,Ocλx,ζ,0=g4x,ζ.

Let us assume that above system of equations has the solution in the series form:

Tdλx,ζ=k=0λkTdλx,ζ,Ecλx,ζ=k=0λkEcλx,ζ,Mcλx,ζ=k=0λkMcλx,ζ,Ocλx,ζ=k=0λkOcλx,ζ.(16)

Operating the RL fractional integral to both sides of the system of equations and using the above assumed initial solutions and Theorem 2.5, we obtain

Tdλx,ζ=g1x+λJtα0Dn2Tdx2χTdxEcx+Td2Ecx2,Ecλx,ζ=g2x+λJtα0ηMcEc,Mcλx,ζ=g3x+λJtα0Dm2Mcx2+kTdσMc,Ocλx,ζ=g4x+λJtα0Dc2Ocx2+EcγωMcɸOc.(17)

Substituting the solution in the series from the above system of equations, we obtain

k=0λkTdλx,ζ=g1x+λJtα0k=0λkDn2Tdkx2χk=0λkTdkxEckx+k=0λkTd2Eckx2,k=0λkEcλx,ζ=g2x+λJtα0k=0λkηMckEck,k=0λkMcλx,ζ=g3x+λJtα0k=0λkDm2Mckx2+k=0λkkTdkk=0λkσMck,k=0λkOcλx,ζ=g4x+λJtα0k=0λkDc2Ockx2+k=0λkEckγk=0λkωMckk=0λkɸOck.(18)

Equating the same powers of λ in Eq. 17, we obtain the following terms:

Td0x,ζ,=g1x,ζ,Ec0x,ζ=g2x,ζ,Mc0x,ζ=g3x,ζ,Oc0x,ζ=g4x,ζ,
Td1x,ζ=Jtα0Dn2Td0x2χTd0xEc0x+Td02Ec0x2,Ec1x,ζ=Jtα0ηMc0Ec0,
Mc1x,ζ=Jtα0Dm2Mc0x2+kTd0σMc0,Oc1x,ζ=Jtα0Dc2Oc0x2+E0γωMc0ɸOc0.Tdkx,ζ=Jtα0Dn2Tdkx2χTdkxEckx+Tdk2Eckx2,Eckx,ζ=Jtα0ηMckEck,
Mckx,ζ=Jtα0Dm2Mckx2+kTdkσMck,Ockx,ζ=Jtα0Dc2Ockx2+EkγωMckɸOck.

Using Eqs 15, 16, we can obtain the solution as

vx,y,t=limλ1vλx,y,t=k=0vkx,y,t.(19)

In Eq. 19, we observe that vx,y,0=limλ1vλx,y,0, which gives gx=vx,y,0.

Considering the terms obtained by solving Eq. 18 and using Eq. 19 and definition 4.3, we have obtained some terms.

By using Mathematica software, the solution was computed, and the 3D and 2D curves were plotted.

Let us considering non-dimensional parameters as γ=0.5; ϵ=0.01;k=1; σ=0; t=0.01; χ=0.01; ω=0.57; ϕ=0.025; η=50; Bc=0.5; Bp=0.0005; and Bn=0.0005.

After applying the parameters mentioned above, we get the solutions:

Td0x,ζ=ex2ϵ,
Ec0x,ζ=10.5ex2ϵ,
Mc0x,ζ=0.5ex2ϵ,
Oc0x,ζ=0.5ex2ϵ,
Td1x,ζ=e2x2ϵBnex2ϵ4x22ϵ+4x2χ1ϵχtαϵ2Γ1+α,
Ec1x,ζ=0.5e2x2ϵ0.5+ex2ϵηtαΓ1+α,
Mc1x,ζ=ex2ϵBp2.x21.ϵ+ϵ2k0.5σtαϵ2Γ1+α,
Oc1x,ζ=1ϵ2Γ1+αγϵ2+ex2ϵBc2.x21.ϵ+ϵ20.5γ0.5ϕ0.5ωtα,
Td2x,ζ=e2x2ϵBnex2ϵ4x22ϵ+4x2χ1ϵχtαϵ2Γ1+α+e3x2ϵt2αϵ4Γ1+2αBn2e2x2ϵ16x448x2ϵ+12ϵ2+ex2ϵBn80x4116x2ϵ+14ϵ2+4x21ϵϵ2ηχ+χx2ϵ6ϵη18χ+24x4χ+ϵ21ϵη+1χ,
Ec2x,ζ=0.5e2x2ϵ0.5+ex2ϵηtαΓ1+α1Γ1+2αe3x2ϵ0.5+ex2ϵt2αη0.25η+ex2ϵk+Bp2x21ϵϵ20.5σ,
Mc2x,ζ=ex2ϵ(Bp2x21ϵ+ϵ2k0.5σtαϵ2Γ1+α+e2x2ϵt2αϵ4Γ1+2α(ex2ϵBnk4x22ϵϵ2+hkhjBp28x424x2ϵ+6ϵ2+ϵ41k+0.5σσ+Bpϵ2(4kx22kϵ4x2σ+2ϵσ+k4x21ϵx21ϵ4ϵ2χ,
Oc2x,ζ=tαex2ϵBc2x21ϵ+ϵ20.5γ0.5ω0.5ϕ+γϵ2ϵ2Γ1+α1ϵ4Γ1+2α(0.5t2αex2ϵ)ϵ2(ϵ(ϵγη1.0.5ex2ϵ+2kω1σω+γϕ2ex2ϵ1+ϕ1ω1ϕ)2.Bpω)+4.Bpx2ω)+Bc2(16x4+48x2ϵ12ϵ2+Bcϵ2ϵ2γ2ω4ϕ+x24γ+4ω+8ϕ).

7 Numerical results and discussion

In this work, an approximate analytical method that is efficient and reliable has been employed. For the analysis of the model under consideration, we utilized the series of the AAM solution. The solutions are shown via graphs to determine the nature of the considered fractional order model. Figure 1 shows the solution for the system of equations in 3D plots at α=1, and it also represents the surface accumulation of the system with respect to x and t. The 3D plot of tumor cell density represents an increase in the number of tumor cells, which results in the breakdown of the extracellular matrix, which is shown in the Fc plot. The matrix-degrading enzymes, which are formed by tumor cells, increase with the increase in tumor cells, as shown in the Mc and Oc plots; this signifies the rate of production of oxygen and its absorption rate by macromolecules. In Figure 2, the behavior and characteristics of the solutions are illustrated for varying x values. From the plots, we can observe that the tumor cells and matrix-degrading enzymes increase with the increase in time, but the extracellular matrix and the rate of production of oxygen decrease. Particularly, enzymes that degrade matrix and extracellular matrix exhibit stimulating behavior for the change α. Additionally, these kinds of research may clear the way for analysis that includes diffusion coefficients into interesting models that illustrate fatal diseases. Figure 3 represents the α curves based on different alpha values. In the present work, we investigated the fractional behavior of the considered model under the influence of the system parameters. Another important observation we made from the plots is that the parameters influence the model’s results in the system and its history. By analyzing the obtained results, we can conclude that the considered method is an efficient tool to analyze the behavior of the model using fractional operators.

Figure 1
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Figure 1. Nature of AAM solution for (A) Td (x, t) (B) Fc (x, t) (C) Mc (x, t) (D) Oc (x, t) (E) Combined surface plot.

Figure 2
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Figure 2. Aquered AAM solution for (A) Td (x, t) (B) Fc (x, t) (C) Mc (x, t) (D) Oc (x, t) (E) Combined surface plot at different alpha values.

Figure 3
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Figure 3. Nature of the solution with respect to time for (A) Td (x, t) (B) Fc (x, t) (C) Mc (x, t) (D) Oc (x, t).

8 Conclusion

The expected analytical solutions for the fractional solid tumor invasion model are studied using an approximate analytical method in the current work. Here, we considered the fractional Caputo derivative to study the considered problem. This method has the potential to be applied to various biological and epidemiological models. The following conclusions can be drawn:

• The uniqueness and existence of the model’s system of solutions with fixed-point theorems are explained.

• The solutions we got using the AAM are in the form of series and converge rapidly.

• The plots indicate a clear influence of both the arbitrary order and the applied parameters on the model.

• The behavior of the model is also dependent on both time instant and time history, which can be easily analyzed by the fractional calculus concept.

• Our analysis confirms that the proposed method is exceptionally efficient and successfully resolves a wide range of non-linear fractional mathematical, biological, and other models.

• The field of mathematical modeling is experiencing a new era with the emergence of fractional calculus.

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 author.

Author contributions

HC: conceptualization, data curation, formal analysis, funding acquisition, investigation, methodology, project administration, resources, software, supervision, writing–original draft, and writing–review and editing. RS: conceptualization, data curation, formal analysis, funding acquisition, investigation, methodology, project administration, resources, software, writing–original draft, and writing–review and editing. DP: investigation, methodology, project administration, resources, software, writing–original draft, writing–review and editing, conceptualization, data curation, formal analysis, and funding acquisition. AQ: conceptualization, data curation, formal analysis, funding acquisition, investigation, methodology, project administration, resources, software, writing–original draft, and writing–review and editing. NM: conceptualization, data curation, formal analysis, funding acquisition, investigation, methodology, project administration, resources, software, writing–original draft, and writing–review and editing. MN: conceptualization, data curation, formal analysis, funding acquisition, investigation, methodology, project administration, resources, software, writing–original draft, and writing–review and editing. DS: conceptualization, data curation, formal analysis, funding acquisition, investigation, methodology, project administration, resources, software, writing–original draft, and writing–review and editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

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.

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.

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Keywords: solid tumor invasion, Rieman–Liouville fractional integral, Caputo fractional derivative, approximate analytical method, differential equations

Citation: Chethan HB, Saadeh R, Prakasha DG, Qazza A, Malagi NS, Nagaraja M and Sarwe DU (2024) An efficient approximate analytical technique for the fractional model describing the solid tumor invasion. Front. Phys. 12:1294506. doi: 10.3389/fphy.2024.1294506

Received: 14 September 2023; Accepted: 26 April 2024;
Published: 04 July 2024.

Edited by:

Ndolane Sene, Cheikh Anta Diop University, Senegal

Reviewed by:

Necati Özdemir, Balıkesir University, Türkiye
Mohamed Abdel Latif, Mansoura University, Egypt

Copyright © 2024 Chethan, Saadeh, Prakasha, Qazza, Malagi, Nagaraja and Sarwe. 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: Rania Saadeh, rsaadeh@zu.edu.jo

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.