Research article Special Issues

Effect of color cross-correlated noise on the growth characteristics of tumor cells under immune surveillance


  • Received: 15 October 2023 Revised: 27 November 2023 Accepted: 30 November 2023 Published: 06 December 2023
  • Based on the Michaelis-Menten reaction model with catalytic effects, a more comprehensive one-dimensional stochastic Langevin equation with immune surveillance for a tumor cell growth system is obtained by considering the fluctuations in growth rate and mortality rate. To explore the impact of environmental fluctuations on the growth of tumor cells, the analytical solution of the steady-state probability distribution function of the system is derived using the Liouville equation and Novikov theory, and the influence of noise intensity and correlation intensity on the steady-state probability distributional function are discussed. The results show that the three extreme values of the steady-state probability distribution function exhibit a structure of two peaks and one valley. Variations of the noise intensity, cross-correlation intensity and correlation time can modulate the probability distribution of the number of tumor cells, which provides theoretical guidance for determining treatment plans in clinical treatment. Furthermore, the increase of noise intensity will inhibit the growth of tumor cells when the number of tumor cells is relatively small, while the increase in noise intensity will further promote the growth of tumor cells when the number of tumor cells is relatively large. The color cross-correlated strength and cross-correlated time between noise also have a certain impact on tumor cell proliferation. The results help people understand the growth kinetics of tumor cells, which can a provide theoretical basis for clinical research on tumor cell growth.

    Citation: Yan Fu, Tian Lu, Meng Zhou, Dongwei Liu, Qihang Gan, Guowei Wang. Effect of color cross-correlated noise on the growth characteristics of tumor cells under immune surveillance[J]. Mathematical Biosciences and Engineering, 2023, 20(12): 21626-21642. doi: 10.3934/mbe.2023957

    Related Papers:

  • Based on the Michaelis-Menten reaction model with catalytic effects, a more comprehensive one-dimensional stochastic Langevin equation with immune surveillance for a tumor cell growth system is obtained by considering the fluctuations in growth rate and mortality rate. To explore the impact of environmental fluctuations on the growth of tumor cells, the analytical solution of the steady-state probability distribution function of the system is derived using the Liouville equation and Novikov theory, and the influence of noise intensity and correlation intensity on the steady-state probability distributional function are discussed. The results show that the three extreme values of the steady-state probability distribution function exhibit a structure of two peaks and one valley. Variations of the noise intensity, cross-correlation intensity and correlation time can modulate the probability distribution of the number of tumor cells, which provides theoretical guidance for determining treatment plans in clinical treatment. Furthermore, the increase of noise intensity will inhibit the growth of tumor cells when the number of tumor cells is relatively small, while the increase in noise intensity will further promote the growth of tumor cells when the number of tumor cells is relatively large. The color cross-correlated strength and cross-correlated time between noise also have a certain impact on tumor cell proliferation. The results help people understand the growth kinetics of tumor cells, which can a provide theoretical basis for clinical research on tumor cell growth.



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    [1] L. B. Han, Influences of time delay on logistic growth process driven by colored correlated noises, Acta Phys. Sin., 57 (2008), 2699–2703. https://doi.org/10.7498/aps.57.2699 doi: 10.7498/aps.57.2699
    [2] Z. L. Jia, Influences of noise correlation and time delay on stochastic resonance induced by multiplicative signal in a cancer growth system, Chin. Phys. B, 19 (2010), 020504. https://doi.org/10.1088/1674-1056/19/2/020504 doi: 10.1088/1674-1056/19/2/020504
    [3] C. J. Wang, Q. Wei, B. B. Zheng, D. C. Mei, Transient properties of a tumor cell growth system driven by color Gaussian noises: Mean first-passage time, Acta Phys. Sin., 57 (2008), 1375–1380. https://doi.org/10.1016/S1872-2075(08)60042-4 doi: 10.1016/S1872-2075(08)60042-4
    [4] M. J. Bie, W. R. Zhong, D. H. Chen, L. Li, Y. Z. Shao, Influence of correlated white noises on the immunity of an anti-tumor system, Acta Phys. Sin., 58 (2009), 97–101. https://doi.org/10.3969/j.issn.1674-697X.2014.07.219 doi: 10.3969/j.issn.1674-697X.2014.07.219
    [5] W. Xu, M. Hao, X. Gu, G. Yang, Stochastic resonance induced by Lévy noise in a tumor growth model with periodic treatment, Mod. Phys. Lett. B, 28 (2014), 1450085. https://doi.org/10.1142/S0217984914500857 doi: 10.1142/S0217984914500857
    [6] T. Yang, Q. Han, C. Zeng, H. Wang, Y. Fu, C. Zhang, Delay-induced state transition and resonance in periodically driven tumor model with immune surveillance, Cent. Eur. J. Phys., 12 (2014), 383–391. https://doi.org/10.2478/s11534-014-0460-0 doi: 10.2478/s11534-014-0460-0
    [7] D. Li, W. Xu, Y. Guo, Y. Xu, Fluctuations induced extinction and stochastic resonance effect in a model of tumor growth with periodic treatment, Phys. Lett. A, 375 (2011), 886–890. https://doi.org/10.1016/j.physleta.2010.12.066 doi: 10.1016/j.physleta.2010.12.066
    [8] P. Han, W. Xu, L. Wang, H. Zhang, S. Ma, Most probable dynamics of the tumor growth model with immune surveillance under cross-correlated noises, Physica A, 547 (2020), 123833. https://doi.org/10.1016/j.physa.2019.123833 doi: 10.1016/j.physa.2019.123833
    [9] W. R. Zhong, Y. Z. Shao, Z. H. He, Stochastic resonance in the growth of a tumor induced by correlated noises, Chin. Sci. Bull., 50 (2005), 2273–2275. https://doi.org/10.1007/BF03183733 doi: 10.1007/BF03183733
    [10] A. Fiasconaro, A. Ochab-Marcinek, B. Spagnolo, E. Gudowska-Nowak, Monitoring noise-resonant effects in cancer growth influenced by external fluctuations and periodic treatment, Eur. Phys. J. B, 65 (2008), 435–442. https://doi.org/10.1140/epjb/e2008-00246-2 doi: 10.1140/epjb/e2008-00246-2
    [11] C. J. Fang, Moment Lyapunov exponent of three-dimensional system under bounded noise excitation, Appl. Math. Mech., 33 (2012), 553–566. https://doi.org/10.1007/sl0483-012-1570-9 doi: 10.1007/sl0483-012-1570-9
    [12] B. Q. Ai, X. J. Wang, G. T. Liu, L. G. Liu, Correlated noise in a logistic growth model, Phys. Rev. E, 67 (2003), 022903. https://doi.org/10.1103/PhysRevE.67.022903 doi: 10.1103/PhysRevE.67.022903
    [13] M. Hua, Y. Wu, Transition in a delayed tumor growth model with non-Gaussian colored noise, Nonlinear Dyn. 111 (2023), 6727–6743. https://doi.org/10.1007/s11071-022-08153-4 doi: 10.1007/s11071-022-08153-4
    [14] H. J. Alsakaji, F. A. Rihan, K. Udhayakumar, F. El Ktaib, Stochastic tumor-immune interaction model with external treatments and time delays: An optimal control problem, Math. Biosci. Eng., 20 (2023), 19270–19299. https://doi.org/10.3934/mbe.2023852 doi: 10.3934/mbe.2023852
    [15] F. A. Rihan, H. J. Alsakaji, S. Kundu, O. Mohamed, Dynamics of a time-delay differential model for tumour-immune interactions with random noise, Alexandria Eng. J., 12 (2022), 11913–11923. https://doi.org/10.1016/j.aej.2022.05.027 doi: 10.1016/j.aej.2022.05.027
    [16] G. Song, T. H. Tian, X. N. Zhang, A mathematical model of cell-mediated immune response to tumor, Math. Biosci. Eng., 18 (2021), 373–385. https://doi.org/10.3934/mbe.2021020 doi: 10.3934/mbe.2021020
    [17] G. W. Wang, D. H. Xu, Q. H. Cheng, Influences of correlated colored-noises on logistic model for tree growth, Acta Phys. Sin., 62 (2013), 224208. https://doi.org/10.7498/aps.62.224208 doi: 10.7498/aps.62.224208
    [18] Z. Jackiewicz, B. Zubik-Kowal, B. Basse, Finite-difference and pseudo-spectral methods for the numerical simulations of in vitro human tumor cell population kinetics, Math. Biosci. Eng., 6 (2009), 561–572. https://doi.org/10.3934/mbe.2009.6.561 doi: 10.3934/mbe.2009.6.561
    [19] I. K. Elena, M. A. de Quesada, C. M. Pérez-Amor, M. L. Texeira, J. M. Nieto-Villar, The dynamics of tumorgrowth and cells pattern morphology, Math. Biosci. Eng., 6 (2009), 547–559. https://doi.org/10.3934/mbe.2009.6.547 doi: 10.3934/mbe.2009.6.547
    [20] Y. F. Guo, T. Yao, L. J. Wang, Lévy noise-induced transition and stochastic resonance in a tumor growth model, Appl. Math. Model., 94 (2021), 506–515. https://doi.org/10.1016/j.apm.2021.01.024 doi: 10.1016/j.apm.2021.01.024
    [21] S. L. Elliott, E. Kose, A. L. Lewis, A. E. Steinfeld, E. A. Zollinger, Modeling the stem cell hypothesis: Investigating the effects of cancer stem cells and TGF-β on tumor growth, Math. Biosci. Eng., 16 (2019), 7177–7194. https://doi.org/10.3934/mbe.2019360 doi: 10.3934/mbe.2019360
    [22] P. Han, W. Xu, L. Wang, H. Zhang, S. Ma, Most probable dynamics of the tumor growth model with immune surveillance under cross-correlated noises, Physica A, 547 (2020), 123833. https://doi.org/10.1016/j.physa.2019.123833 doi: 10.1016/j.physa.2019.123833
    [23] A. Fiasconaro, B. Spagnolo, A. Ochab-Marcinek, E. Gudowska-Nowak, Co-occurrence of resonant activation and noise enhanced stability in a model of cancer growth in the presence of immune response, Phys. Rev. E, 74 (2006), 041904. https://doi.org/10.1103/PhysRevE.74.041904 doi: 10.1103/PhysRevE.74.041904
    [24] X. Chen, T. D. Li, W. Cao, Optimizing cancer therapy for individuals based on tumor-immune-drug system interaction, Math. Biosci. Eng., 20 (2023), 17589–17607. https://doi.org/10.3934/mbe.2023781 doi: 10.3934/mbe.2023781
    [25] M. Assaf, E. Roberts, Z. Luthey-Schulten, Determining the stability of genetic switches, explicitly accounting for mRNA noise, Phys. Rev. Lett., 106 (2011), 248102. https://doi.org/10.1103/PhysRevLett.106.248102 doi: 10.1103/PhysRevLett.106.248102
    [26] G. W. Wang, M. Y. Ge, L. L. Lu, Y. Jia, Y. Zhao, Study on propagation efficiency and fidelity of subthreshold signal in feed-forward hybrid neural network under electromagnetic radiation, Nonlinear Dyn., 103 (2021), 2627–2643. https://doi.org/10.1007/s11071-021-06247-z doi: 10.1007/s11071-021-06247-z
    [27] X. Zhao, Q. Ouyang, H. Wang, Designing a stochastic genetic switch by coupling chaos and bistability, Chaos, 25 (2015), 113112. https://doi.org/10.1063/1.4936087 doi: 10.1063/1.4936087
    [28] M. J. Bie, W. R. Zhong, H. D. Chen, L. Li, Y. Z. Shao, Effect of the associated white noise against the immune effect of the tumor system, Acta Phys. Sin., 58 (2009), 97–101. https://doi.org/10.7498/aps.58.97 doi: 10.7498/aps.58.97
    [29] A. I. Reppas, J. C. L. Alfonso, H. Hatzikirou, In silico tumor control induced via alternating immunostimulating and immunosuppressive phases, Virulence, 7 (2016), 174–186. https://doi.org/10.1080/21505594.2015.1076614 doi: 10.1080/21505594.2015.1076614
    [30] Y. Jia, J. R. Li, Steady-state analysis of a bistable system with additive and multiplicative noises, Phys. Rev. E, 53 (1996), 5786–5792. https://doi.org/10.1103/PhysRevE.53.5786 doi: 10.1103/PhysRevE.53.5786
    [31] Q. Liu, Y. Jia, Fluctuations-induced switch in the gene transcriptional regulatory system, Phys. Rev. E, 70 (2004), 041907. https://doi.org/10.1103/PhysRevE.70.041907 doi: 10.1103/PhysRevE.70.041907
    [32] Y. Li, M. Yi, X. Zou, The linear interplay of intrinsic and extrinsic noises ensures a high accuracy of cell fate selection in budding yeast, Sci. Rep., 4 (2014), 1–13. https://doi.org/10.1038/srep05764 doi: 10.1038/srep05764
    [33] Y. Xu, J. Feng, J. Li, H. Zhang, Lévy noise induced switch in the gene transcriptional regulatory system, Chaos, 23 (2013), 013110. https://doi.org/10.1063/1.4775758 doi: 10.1063/1.4775758
    [34] A. M. Edwards, R. A. Phillips, N. W. Watkins, M. P. Freeman, E. J. Murphy, V. Afanasyev, et al., Revisiting Lévy flight search patterns of wandering albatrosses, bumblebees and deer, Nature, 449 (2007), 1044–1048. https://doi.org/10.1038/nature06199 doi: 10.1038/nature06199
    [35] C. Wang, M. Yi, K. Yang, L. Yang, Time delay induced transition of gene switch and stochastic resonance in a genetic transcriptional regulatory model, BMC Syst. Biol., 6 (2012), 1–16. https://doi.org/10.1186/1752-0509-6-S1-S9 doi: 10.1186/1752-0509-6-S1-S9
    [36] G. W. Wang, Y. Fu, Spatiotemporal patterns and collective dynamics of bi-layer coupled Izhikevich neural networks with multi-area channels, Math. Biosci. Eng., 20 (2023), 3944–3969. https://doi.org/10.3934/mbe.2023184 doi: 10.3934/mbe.2023184
    [37] H. C. Wei, Mathematical modeling of tumor growth: the MCF-7 breast cancer cell line, Math. Biosci. Eng., 16 (2019), 6512–6535. https://doi.org/10.3934/mbe.2019325 doi: 10.3934/mbe.2019325
    [38] G. W. Wang, Y. Fu, Modes transition and network synchronization in extended Hindmarsh–Rose model driven by mutation of adaptation current under effects of electric field, Indian J. Phys., 97 (2023), 2327–2337. https://doi.org/10.1007/s12648-023-02613-2 doi: 10.1007/s12648-023-02613-2
    [39] C. H. Zeng, H. Wang, Colored noise enhanced stability in a tumor cell growth system under immune response, J. Stat. Phys., 141 (2010), 889–908. https://doi.org/10.1007/s10955-010-0068-8 doi: 10.1007/s10955-010-0068-8
    [40] A. Ochab-Marcinek, A. Fiasconaro, E. Gudowska-Nowak, B. Spagnolo, Coexistence of resonant activation and noise enhanced stability in a model of tumor-host interaction Statistics of extinction times, Acta Phys. Pol. B, 37 (2006), 1651–1666. https://doi.org/10.1051/esomat/200905011 doi: 10.1051/esomat/200905011
    [41] B. Spagnolo, A. Fiasconaro, N. Pizzolato, D. Valenti, D. P. Adorno, P. Caldara, et al., Cancer growth dynamics: stochastic models and noise induced effects, AIP Conf. Proc., 1129 (2009), 539–544. https://doi.org/10.1063/1.3140529 doi: 10.1063/1.3140529
    [42] T. Y. Li, G. W. Wang, D. Yu, Q. Ding, Y. Jia, Synchronization mode transitions induced by chaos in modified Morris-Lecar neural systems with weak coupling, Nonlinear Dyn., 108 (2022), 2611–2625. https://doi.org/10.1007/s11071-022-07318-5 doi: 10.1007/s11071-022-07318-5
    [43] T. Tashiro, K. Imamura, Y. Tomita, D. Tamanoi, A. Takaki, K. Sugahara, et al., Heterogeneous tumor-immune microenvironments between primary and metastatic tumors in a patient with ALK rearrangement-positive large cell neuroendocrine carcinoma, Int. J. Mol. Sci., 21 (2020), 9705. https://doi.org/10.3390/ijms21249705 doi: 10.3390/ijms21249705
    [44] D. Liu, S. Ruan, D. Zhu, Bifurcation analysis in models of tumor and immune system interactions, Discrete Contin. Dyn. Syst., 12 (2012), 151–168. https://doi.org/10.3934/dcdsb.2009.12.151 doi: 10.3934/dcdsb.2009.12.151
    [45] G. W. Wang, L. J. Yang, X. Zhan, A. Li, Y. Jia, Chaotic resonance in Izhikevich neural network motifs under electromagnetic induction, Nonlinear Dyn., 107 (2022), 3945–3962. https://doi.org/10.1007/s11071-021-07150-3 doi: 10.1007/s11071-021-07150-3
    [46] H. Mayer, K. S. Zaenker, U. A. D. Heiden, A basic mathematical model of the immune response, Chaos, 5 (1995), 155–161. https://doi.org/10.1063/1.166098 doi: 10.1063/1.166098
    [47] N. Burić, M. Mudrinic, N. Vasovićet, Time delay in a basic model of the immune response, Chaos, Solitons Fractals, 12 (2001), 483–489. https://doi.org/10.1016/S0960-0779(99)00205-2 doi: 10.1016/S0960-0779(99)00205-2
    [48] C. Yu, J. Wei, Stability and bifurcation analysis in a basic model of the immune response with delays, Chaos, Solitons Fractals, 41 (2009), 1223–1234. https://doi.org/10.1016/j.chaos.2008.05.007 doi: 10.1016/j.chaos.2008.05.007
    [49] H. Wang, X. Tian, Asymptotic properties and stability switch of a delayed-within-host-dengue infection model with mitosis and immune response, Int. J. Bifurcation Chaos, 8 (2022), 32. https://doi.org/10.1142/S0218127422501188 doi: 10.1142/S0218127422501188
    [50] D. Yu, G. W. Wang, T. Y. Li, Q. Ding, Y. Jia, Filtering properties of Hodgkin-Huxley neuron on different time-scale signals, Commun. Nonlinear Sci., 117 (2023), 106894. https://doi.org/10.1016/j.cnsns.2022.106894 doi: 10.1016/j.cnsns.2022.106894
    [51] G. W. Wang, D. Yu, Q. M. Ding, T. Li, Y. Jia, Effects of electric field on multiple vibrational resonances in Hindmarsh-Rose neuronal systems, Chaos, Solitons Fractals, 150 (2021), 111210. https://doi.org/10.1016/j.chaos.2021.111210 doi: 10.1016/j.chaos.2021.111210
    [52] S. Asserda, A. Bernoussi, M. E. Fatini, A. Kaddar, A. Laaribi, On the dynamics of a delayed tumor-immune model, Int. J. Ecol. Econ. Stat., 33 (2014), 20–30.
    [53] A. Kaddar, H. T. Alaoui, Global existence of periodic solutions in a delayed tumor-immune model, Math. Model. Nat. Phenom., 5 (2010), 29–34. https://doi.org/10.1051/mmnp/20105705 doi: 10.1051/mmnp/20105705
    [54] G. W. Wang, Y. Wu, F. L. Xiao, Z. Ye, Y. Jia, Non-Gaussian noise and autapse-induced inverse stochastic resonance in bistable Izhikevich neural system under electromagnetic induction, Physica A, 598 (2022), 127274. https://doi.org/10.1016/j.physa.2022.12727 doi: 10.1016/j.physa.2022.12727
    [55] K. Wang, Y. Jin, A. Fan, The effect of immune responses in viral infections: A mathematical model view, Discrete Contin. Dyn. Syst., 19 (2017), 3379–3396. https://doi.org/10.1007/s00285-010-0397-x doi: 10.1007/s00285-010-0397-x
    [56] A. Bukkuri, A mathematical model showing the potential of Vitamin-C to boost the innate immune response, Open J. Math. Sci., 3 (2019), 245–255. https://doi.org/10.30538/oms2019.0067 doi: 10.30538/oms2019.0067
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