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10.3390/biom11010065

http://scihub22266oqcxt.onion/10.3390/biom11010065
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33419007!7825278!33419007
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suck abstract from ncbi

pmid33419007      Biomolecules 2021 ; 11 (1): ?
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  • Endolysosomal TRPMLs in Cancer #MMPMID33419007
  • Xu M; Dong XP
  • Biomolecules 2021[Jan]; 11 (1): ? PMID33419007show ga
  • Lysosomes, the degradative endpoints and sophisticated cellular signaling hubs, are emerging as intracellular Ca(2+) stores that govern multiple cellular processes. Dys-homeostasis of lysosomal Ca(2+) is intimately associated with a variety of human diseases including cancer. Recent studies have suggested that the Ca(2+)-permeable channels Transient Receptor Potential (TRP) Mucolipins (TRPMLs, TRPML1-3) integrate multiple processes of cell growth, division and metabolism. Dysregulation of TRPMLs activity has been implicated in cancer development. In this review, we provide a summary of the latest development of TRPMLs in cancer. The expression of TRPMLs in cancer, TRPMLs in cancer cell nutrient sensing, TRPMLs-mediated lysosomal exocytosis in cancer development, TRPMLs in TFEB-mediated gene transcription of cancer cells, TRPMLs in bacteria-related cancer development and TRPMLs-regulated antitumor immunity are discussed. We hope to guide readers toward a more in-depth discussion of the importance of lysosomal TRPMLs in cancer progression and other human diseases.
  • |Animals[MESH]
  • |Autophagy/genetics[MESH]
  • |Endosomes/*metabolism[MESH]
  • |Humans[MESH]
  • |Immunity/genetics[MESH]
  • |Lysosomes/*metabolism[MESH]
  • |Neoplasms/genetics/immunology/*metabolism[MESH]


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