RRC ID 77491
著者 Ueda Y, Miura Y, Tomishige N, Sugimoto N, Murase M, Kawamura G, Sasaki N, Ishiwata T, Ozawa T.
タイトル Mechanistic insights into cancer drug resistance through optogenetic PI3K signaling hyperactivation.
ジャーナル Cell Chem Biol
Abstract Hyperactivation of phosphatidylinositol 3-kinase (PI3K) signaling is a prominent feature in cancer cells. However, the mechanism underlying malignant behaviors in the state remains unknown. Here, we describe a mechanism of cancer drug resistance through the protein synthesis pathway, downstream of PI3K signaling. An optogenetic tool (named PPAP2) controlling PI3K signaling was developed. Melanoma cells stably expressing PPAP2 (A375-PPAP2) acquired resistance to a cancer drug in the hyperactivation state. Proteome analyses revealed that expression of the antiapoptotic factor tumor necrosis factor alpha-induced protein 8 (TNFAIP8) was upregulated. TNFAIP8 upregulation was mediated by protein translation from preexisting mRNA. These results suggest that cancer cells escape death via upregulation of TNFAIP8 expression from preexisting mRNA even though alkylating cancer drugs damage DNA.
巻・号 29(11)
ページ 1576-1587.e5
公開日 2022-11-17
DOI 10.1016/j.chembiol.2022.10.002
PII S2451-9456(22)00356-7
PMID 36288730
MeSH Cell Line, Tumor Drug Resistance, Neoplasm Neoplasms* / drug therapy Optogenetics Phosphatidylinositol 3-Kinases* / metabolism Proto-Oncogene Proteins c-akt / metabolism RNA, Messenger Signal Transduction
IF 6.762
リソース情報
遺伝子材料 tFucci(CA)2.2/pCSII-CMV (RDB15454) Lenti-pCSII-CMV-PPAP2.1-IRES-puro(Amp) (RDB20343) Lenti-pCSII-CMV-PPAP2.2-IRES-puro(Amp) (RDB20663) pCAG-His-iSH-SspB-P2AT2A-mVenus-iLID-CAAX (RDB20664) pCAGkawa-His-iSH-SspB-mCherry-P2AT2A-iLID-CAAX (RDB20665)