| Literature DB >> 29669935 |
Sha Zhu1, B Marie Ward2, Jun Yu1, Asia N Matthew-Onabanjo1, Jenny Janusis1, Chung-Cheng Hsieh1, Keith Tomaszewicz3, Lloyd Hutchinson3, Lihua Julie Zhu1,4,5, Dina Kandil3, Leslie M Shaw1.
Abstract
Pleomorphic invasive lobular carcinoma (PILC) is an aggressive variant of invasive lobular breast cancer that is associated with poor clinical outcomes. Limited molecular data are available to explain the mechanistic basis for PILC behavior. To address this issue, targeted sequencing was performed to identify molecular alterations that define PILC. This sequencing analysis identified genes that distinguish PILC from classic ILC and invasive ductal carcinoma by the incidence of their genomic changes. In particular, insulin receptor substrate 2 (IRS2) is recurrently mutated in PILC, and pathway analysis reveals a role for the insulin receptor (IR)/insulin-like growth factor-1 receptor (IGF1R)/IRS2 signaling pathway in PILC. IRS2 mutations identified in PILC enhance invasion, revealing a role for this signaling adaptor in the aggressive nature of PILC.Entities:
Keywords: Breast cancer; Insulin signaling; Oncology
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Year: 2018 PMID: 29669935 PMCID: PMC5931118 DOI: 10.1172/jci.insight.97398
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708