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10.1016/j.canlet.2016.03.033

http://scihub22266oqcxt.onion/10.1016/j.canlet.2016.03.033
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C5107316!5107316 !27039259
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suck abstract from ncbi


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pmid27039259
      Cancer+Lett 2016 ; 379 (2 ): 166-72
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  • TGF-? signaling in liver and gastrointestinal cancers #MMPMID27039259
  • Katz LH ; Likhter M ; Jogunoori W ; Belkin M ; Ohshiro K ; Mishra L
  • Cancer Lett 2016[Sep]; 379 (2 ): 166-72 PMID27039259 show ga
  • Transforming Growth Factor-? (TGF-?) plays crucial and complex roles in liver and gastrointestinal cancers. These include a multitude of distinct functions, such as maintaining stem cell homeostasis, promoting fibrosis, immune modulating, as a tumor suppressor and paradoxically, as a tumor progressor. However, key mechanisms for the switches responsible for these distinct actions are poorly understood, and remain a challenge. The Cancer Genome Atlas (TCGA) analyses and genetically engineered mouse models now provide an integrated approach to dissect these multifaceted and context-dependent driving roles of the TGF-? pathway. In this review, we will discuss the molecular mechanisms of TGF-? signaling, focusing on colorectal, gastric, pancreatic, and liver cancers. Novel drugs targeting the TGF-? pathway have been developed over the last decade, and some have been proven effective in clinical trials. A better understanding of the TGF-? pathway may improve our ability to target it, thus providing more tools to the armamentarium against these deadly cancers.
  • |*Signal Transduction/drug effects [MESH]
  • |Animals [MESH]
  • |Antineoplastic Agents/therapeutic use [MESH]
  • |Gastrointestinal Neoplasms/drug therapy/genetics/*metabolism/pathology [MESH]
  • |Gene Expression Regulation, Neoplastic [MESH]
  • |Humans [MESH]
  • |Liver Neoplasms/drug therapy/genetics/*metabolism/pathology [MESH]
  • |Molecular Targeted Therapy [MESH]
  • |Mutation [MESH]
  • |Neoplastic Stem Cells/metabolism [MESH]
  • |Receptors, Transforming Growth Factor beta/antagonists & inhibitors/metabolism [MESH]


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