Tamar Bar Ziv

ORCID: 0009-0008-1751-8507
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About
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Research Areas
  • Protein Kinase Regulation and GTPase Signaling
  • PI3K/AKT/mTOR signaling in cancer
  • Cancer therapeutics and mechanisms
  • ATP Synthase and ATPases Research
  • Receptor Mechanisms and Signaling
  • Melanoma and MAPK Pathways

Revolution Medicines (United States)
2023-2024

Technion – Israel Institute of Technology
2024

Abstract RAS oncogenes (collectively NRAS , HRAS and especially KRAS ) are among the most frequently mutated genes in cancer, with common driver mutations occurring at codons 12, 13 61 1 . Small molecule inhibitors of KRAS(G12C) oncoprotein have demonstrated clinical efficacy patients multiple cancer types led to regulatory approvals for treatment non-small cell lung 2,3 Nevertheless, G12C account only around 15% -mutated cancers 4,5 there no approved majority tumours containing other...

10.1038/s41586-024-07205-6 article EN cc-by Nature 2024-04-08

Abstract Background Although GqPCR activation often leads to cell survival by activating the PI3K/AKT pathway, it was previously shown that in several types AKT activity is reduced and JNK apoptosis. The mechanism of inactivation these cells involves an IGBP1-coupled PP2Ac switch induces dephosphorylation both PI3K AKT. However, machinery involved initiation PP2A not known. Methods We used phospho-mass spectrometry identify phosphorylation site PP2Ac, raised specific antibodies follow...

10.1186/s12964-024-01536-7 article EN cc-by Cell Communication and Signaling 2024-02-28

Abstract RAS oncogenes (collectively NRAS , HRAS and especially KRAS ) are among the most frequently mutated genes in cancer, with common driver mutations occurring at codons 12, 13 61 1 . Small molecule inhibitors of G12C oncoprotein have demonstrated clinical efficacy patients multiple cancer types led to regulatory approvals for treatment non-small-cell lung (NSCLC) 2,3 Nevertheless, account only ~14% cancers 4 there no approved majority tumors harboring other mutations. Here, we describe...

10.21203/rs.3.rs-3122478/v1 preprint EN cc-by Research Square (Research Square) 2023-07-07
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