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10.1007/978-3-030-12457-1_20

http://scihub22266oqcxt.onion/10.1007/978-3-030-12457-1_20
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31646523!?!31646523

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suck abstract from ncbi

pmid31646523      Adv+Exp+Med+Biol 2020 ; 1131 (?): 505-517
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  • Calcium Signaling and the Regulation of Chemosensitivity in Cancer Cells: Role of the Transient Receptor Potential Channels #MMPMID31646523
  • Santoni G; Morelli MB; Marinelli O; Nabissi M; Santoni M; Amantini C
  • Adv Exp Med Biol 2020[]; 1131 (?): 505-517 PMID31646523show ga
  • Cancer cells acquire the ability to modify the calcium signaling network by altering the expression and functions of cation channels, pumps or transporters. Calcium signaling pathways are involved in proliferation, angiogenesis, invasion, immune evasion, disruption of cell death pathways, ECM remodelling, epithelial-mesenchymal transition (EMT) and drug resistance. Among cation channels, a pivotal role is played by the Transient Receptor Potential non-selective cation-permeable receptors localized in plasma membrane, endoplasmic reticulum, mitochondria and lysosomes. Several findings indicate that the dysregulation in calcium signaling induced by TRP channels is responsible for cancer growth, metastasis and chemoresistance. Drug resistance represents a major limitation in the application of current therapeutic regimens and several efforts are spent to overcome it. Here we describe the ability of Transient Receptor Potential Channels to modify, by altering the intracellular calcium influx, the cancer cell sensitivity to chemotherapeutic drugs.
  • |*Calcium Signaling[MESH]
  • |*Neoplasms/drug therapy/genetics[MESH]
  • |*Transient Receptor Potential Channels/genetics/metabolism[MESH]
  • |Antineoplastic Agents/therapeutic use[MESH]
  • |Calcium/metabolism[MESH]
  • |Drug Resistance, Neoplasm[MESH]


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