Genomic and expression analyses define MUC17 and PCNX1 as predictors of chemotherapy response in breast cancer

Poor prognosis breast cancers are treated with cytotoxic chemotherapy, but often without any guidance from therapy predictive markers since universally-accepted markers are not currently available. Treatment failure, in the form of recurrences, is relatively common. We aimed to identify chemotherapy...

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Hauptverfasser: Al Amri, WS, Allinson, LM, Baxter, DE, Bell, SM, Hanby, AM, Jones, SJ, Shaaban, AM, Stead, LF, Verghese, ET, Hughes, TA
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Sprache:eng
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Zusammenfassung:Poor prognosis breast cancers are treated with cytotoxic chemotherapy, but often without any guidance from therapy predictive markers since universally-accepted markers are not currently available. Treatment failure, in the form of recurrences, is relatively common. We aimed to identify chemotherapy predictive markers and resistance pathways in breast cancer. Our hypothesis was that tumour cells remaining after neoadjuvant chemotherapy (NAC) contain somatic variants causing therapy resistance, while variants present pre-NAC but lost post-NAC cause sensitivity. Whole exome sequencing was performed on matched pre- and post-NAC cancer cells, which were isolated by laser microdissection, from 6 cancer cases, and somatic variants selected for or against by NAC were identified. Somatic variant diversity was significantly reduced after therapy (p
DOI:10.1158/1535-7163.MCT-19-0940