📚 Hub Books: Онлайн-чтение книгМедицинаПарадоксы эволюции. Как наличие ресурсов и отсутствие внешних угроз приводит к самоуничтожению вида и что мы можем с этим сделать - Алексей Аркадьевич Макарушин

Парадоксы эволюции. Как наличие ресурсов и отсутствие внешних угроз приводит к самоуничтожению вида и что мы можем с этим сделать - Алексей Аркадьевич Макарушин

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driver mutations. Proc Natl Acad Sci U S A.; 115 (26): E6010–E6019.

7. Soto A. M., Sonnenschein C. (1999). The Society of cells – Cancer and control of cell proliferation. – Bios Scientific-Springer Verlag, Oxford-NY.

8. Sonnenschein C., Soto A.M. (2008). Theories of carcinogenesis: an emerging perspective. Semin Cancer Biol.; 18 (5): 372–7.

9. Soto A. M., Sonnenschein C. (2011). The tissue organization field theory of cancer: A testable replacement for the somatic mutation theory. Bioessays 33: 332–340.

10. Driesch H. (1908). The Science and Philosophy of the Organism: The Gifford Lectures delivered before the University of Aberdeen in the Year 1907 and 1908 (2 vols.). London: Adam and Charles Black. [1] 2nd ed. London: A. & C. Black, 1929.

11. Mintz B., Illmensee K. (1975). Normal genetically mosaic mice produced from malignant teratocarcinoma cells. Proc Natl Acad SciUSA. 72 (9): 3585–9.

12. Van Wijk R., Van Wijk E. P. A., Pang J., Yang M., Yan Y., Han J. (2020). Integrating Ultra-Weak Photon Emission Analysis in Mitochondrial Research. Front. Physiol. 11: 717.

13. Frankenburger W. (1933). Neuere Ansichten über das Wesen photochemischer Prozesse und ihre Bedeutung zu biologischen Vorgangen. Strahlentherapie. Bd. 47, S. 2.

14. Mattei T. A. (2015). Alternating electric fields and carcinogenesis: a new paradigm to avoid missing the elephant in the room. World Neurosurgery, 83 (5): 718–22.

15. Rosenfeld S. (2013a). Global consensus Theorem and self-Organized criticality: Unifying principles for Understanding self-Organization, swarm Intelligence and Mechanisms of carcinogenesis. Gene Regulation and Systems Biology, 2013: 723–39.

16. Rosenfeld S. (2013b). Are the somatic mutation and tissue organization field theories of Carcinogenesis Incompatible? Cancer Informatics, 12: 221–229.

17. Grossberg S. (1978) Competition, Decision and Consensus. J Math Anal Appl 662: 470-493.

18. Hickson J., Diane Y. S., Berger J., Alverdy J., O’Keefe J., Bassler B, Rinker-Schaeffer C. (2009). Soci et al. interactionsin ovarian cancer metastasis: a quorum-sensing hypothesis. Clin Exp Metastasis, 26: 67–76.

19. Agur Z., Kogan Y., Levi L., Harrison H., Lamb R., Kirnasovsky O. U., Clark R. B. (2010). Disruption of a Quorum Sensing mechanism triggers tumorigenesis: a simple discrete model corroborated byexperiments in mammary cancer stem cells. Biol Direct, 5: 20.

20. Milstein J.N., Meiners J.-C. (2011). On the role of DNA biomechanics in the regulation of gene expression. J. R. Soc. Interface 8, 1673–1681.

21. Toufektchan E., Toledo F. (2018). The Guardian of the Genome Revisited: p53 Downregulates Genes Required for Telomere Maintenance, DNA Repair, and Centromere Structure. Cancers. 10 (5): 135.

22. Nithipongvanitch R., Ittarat W., Velez J. M., Zhao R., St Clair D. K., Oberley T. D. (2007). Evidence for p53 as guardian of the cardiomyocyte mitochondrial genome following acute adriamycin treatment. J. Histochem. Cytochem. 55 (6): 629–639.

23. Vincent A. S., Phan T. T., Mukhopadhyay A., Lim H. Y., Halliwell B., Wong K. P. (2008). Human skin keloid fibroblasts display bioenergetics of cancer cells. J. Invest. Dermatol. 128 702–709.

24. Pavlides S., Whitaker-Menezes D., Castello-Cros R., Flomenberg N., Witkiewicz A. K., Frank P. G., Casimiro M. C., Wang C., Fortina P., Addya S., Pestell R. G., Martinez-Outschoorn U. E., Sotgia F., Lisanti M. P. (2009). The reverse Warburg effect: aerobic glycolysis in cancer associated fibroblasts and the tumor stroma. Cell Cycle, 8 (23): 3984–4001.

25. Martinez-Outschoorn U. E., Balliet R. M., Rivadeneira D. B., Chiavarina B., Pavlides S., Wang C., Whitaker-Menezes D., Daumer K. M., Lin Z., Witkiewicz A. K., Flomenberg N., Howell A., Pestell R. G., Knudsen E. S., Sotgia F., Lisanti M. P. (2010). Oxidative stress in cancer associated fibroblasts drives tumor-stroma co-evolution: A new paradigm for understanding tumor metabolism, the field effect and genomic instability in cancer cells. Cell cycle (Georgetown, Tex.), 9 (16): 3256–3276.

26. Pokorný J., Pokorny J., Kobilková J., Jandová A., Holaj, R. (2020). Cancer Development and Damped Electromagnetic Activity. Applied Sciences, 10, 1826.

27. Fang Z., Xu J., Zhang B., Wang W., Liu J., Liang C., Hua J., Meng Q., Yu X., Shi S. (2020). The promising role of noncoding RNAs in cancer-associated fibroblasts: an overview of current status and future perspectives. J Hematol Oncol 13, 154.

28. Zhao H., Yang L., Baddour J., Achreja A., Bernard V., Moss T., Marini J. C., Tudawe T., Seviour E. G., San Lucas F. A., Alvarez H., Gupta S., Maiti S. N., Cooper L., Peehl D., Ram P. T., Maitra A., Nagrath D. (2016). Tumormicroenvironment derived exosomes pleiotropically modulate cancercell metabolism. Elife, 5: e10250.

29. Zhang H., Deng T., Liu R., Ning T., Yang H., Liu D., Zhang Q., Lin D., Ge S., Bai M., Wang X., Zhang L., Li H., Yang Y., Ji Z., Wang H., Ying G., Ba Y. (2020). CAF secreted miR-522 suppresses ferroptosis and promotes acquired chemo-resistance ingastric cancer. Mol Cancer, 19: 43.

30. Conciatori F., Bazzichetto C., Falcone I., Pilotto S., Bria E., Cognetti F., Milella M., Ciuffreda L. (2018). Role of mTOR Signaling in Tumor Microenvironment: An Overview. International journal of molecular sciences, 19 (8), 2453.

31. Akman M., Belisario D. C., Salaroglio I. C., Kopecka J., Donadelli M., De Smaele E., Riganti C. (2021). Hypoxia, endoplasmic reticulum stress and chemoresistance: dangerous liaisons. J Exp Clin Cancer Res, 11; 40 (1): 28.

32. Ippolito L., Morandi A., Taddei M. L., Parri M., Comito G., Iscaro A., Raspollini M. R., Magherini F., Rapizzi E., Masquelier J., Muccioli G. G., Sonveaux P., Chiarugi P., Giannoni E. (2019). Cancer-associated fibroblasts promote prostate cancer malignancy via metabolic rewiring and mitochondrial transfer. Oncogene, 38 (27): 5339–5355.

33. Liu D., Gao Y., Liu J., Huang Y., Yin J., Feng, Y., Shi L., Meloni B. P., Zhang C., Zheng M., Gao J. (2021). Intercellular mitochondrial transfer as a means of tissue revitalization. Signal Transduction and Targeted Therapy, 6 (1): 65.

34. Zampieri L. X., Silva-Almeida C., Rondeau J. D., Sonveaux P. (2021). Mitochondrial Transfer in Cancer: A Comprehensive Review. Int. J. Mol. Sci., 22, 3245.

35. Dong L. F., Kovarova J., Bajzikova M., Bezawork-Geleta A., Svec D., Endaya B., Sachaphibulkij K., Coelho A. R., Sebkova N., Ruzickova A., Tan A. S., Kluckova K., Judasova K., Zamecnikova K., Rychtarcikova Z., Gopalan V., Andera L., Sobol M., Yan B., Pattnaik B., Bhatraju N., Truksa J., Stopka P., Hozak P., Lam A. K., Sedlacek R., Oliveira P. J., Kubista M., Agrawal A., Dvorakova-Hortova K., Rohlena J.,

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