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Multi-institutional study of nuclear KIFC1 as a biomarker of poor prognosis in African American women with triple-negative breast cancer

Nuclear KIFC1 (nKIFC1) predicts worse outcomes in breast cancer, but its prognostic value within racially distinct triple-negative breast cancer (TNBC) patients is unknown. Thus, nKIFC1 expression was assessed by immunohistochemistry in 163 African American (AA) and 144 White TNBC tissue microarrays...

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Detalles Bibliográficos
Autores principales: Ogden, Angela, Garlapati, Chakravarthy, Li, Xiaoxian (Bill), Turaga, Ravi Chakra, Oprea-Ilies, Gabriela, Wright, Nikita, Bhattarai, Shristi, Mittal, Karuna, Wetherilt, Ceyda Sönmez, Krishnamurti, Uma, Reid, Michelle D., Jones, Mildred, Gupta, Meenakshi, Osan, Remus, Pattni, Sonal, Riaz, Ansa, Klimov, Sergey, Rao, Arundhati, Cantuaria, Guilherme, Rida, Padmashree C. G., Aneja, Ritu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316996/
https://www.ncbi.nlm.nih.gov/pubmed/28218233
http://dx.doi.org/10.1038/srep42289
Descripción
Sumario:Nuclear KIFC1 (nKIFC1) predicts worse outcomes in breast cancer, but its prognostic value within racially distinct triple-negative breast cancer (TNBC) patients is unknown. Thus, nKIFC1 expression was assessed by immunohistochemistry in 163 African American (AA) and 144 White TNBC tissue microarrays (TMAs) pooled from four hospitals. nKIFC1 correlated significantly with Ki67 in White TNBCs but not in AA TNBCs, suggesting that nKIFC1 is not merely a surrogate for proliferation in AA TNBCs. High nKIFC1 weighted index (WI) was associated with significantly worse overall survival (OS), progression-free survival (PFS), and distant metastasis-free survival (DMFS) (Hazard Ratios [HRs] = 3.5, 3.1, and 3.8, respectively; P = 0.01, 0.009, and 0.007, respectively) in multivariable Cox models in AA TNBCs but not White TNBCs. Furthermore, KIFC1 knockdown more severely impaired migration in AA TNBC cells than White TNBC cells. Collectively, these data suggest that nKIFC1 WI an independent biomarker of poor prognosis in AA TNBC patients, potentially due to the necessity of KIFC1 for migration in AA TNBC cells.