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Cited 28 time in webofscience Cited 29 time in scopus
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MMP11 and CD2 as novel prognostic factors in hormone receptor-negative, HER2-positive breast cancer

Authors
Han, J[Han, Jinil]Choi, YL[Choi, Yoon-La]Kim, H[Kim, Haein]Choi, JY[Choi, Jun Young]Lee, SK[Lee, Se Kyung]Lee, JE[Lee, Jeong Eon]Choi, JS[Choi, Joon-Seok]Park, S[Park, Sarah]Choi, JS[Choi, Jong-Sun]Kim, YD[Kim, Young Deug]Nam, SJ[Nam, Seok Jin]Nam, BH[Nam, Byung-Ho]Kwon, MJ[Kwon, Mi Jeong]Shin, YK[Shin, Young Kee]
Issue Date
Jul-2017
Publisher
SPRINGER
Keywords
Breast cancer; Hormone receptor negative; HER2-positive (HR-/HER2+) breast cancer; Prognostic model; Risk of distant metastasis; Immune response-related genes (i-genes); Proliferation-related genes (p-genes)
Citation
BREAST CANCER RESEARCH AND TREATMENT, v.164, no.1, pp.41 - 56
Indexed
SCIE
SCOPUS
Journal Title
BREAST CANCER RESEARCH AND TREATMENT
Volume
164
Number
1
Start Page
41
End Page
56
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/28260
DOI
10.1007/s10549-017-4234-4
ISSN
0167-6806
Abstract
Purpose More accurate prediction of patient outcome based on molecular subtype is required to identify patients who will benefit from specific treatments. Methods We selected novel 16 candidate prognostic genes, including 10 proliferation-related genes (p-genes) and 6 immune response-related genes (i-genes), from the gene list identified in our previous study. We then analyzed the association between their expression, measured by quantitative real-time reverse transcription-PCR in formalin-fixed, paraffin-embedded tissues, and clinical outcome in 819 breast cancer patients according to molecular subtype. Results The prognostic significance of clinical and gene variables varied according to the molecular subtype. Univariate analysis showed that positive lymph node status was significantly correlated with the increased risk of distant metastasis in all subtypes except the hormone receptor-negative, HER2-positive (HR-/HER2+) subtype. Most p-genes were significantly associated with poor prognosis in patients with the HR+/HER2- subtype, whereas i-genes correlated with a favorable outcome in patients with HR-/HER2+ breast cancer. In HR-/HER2+ breast cancer, four genes (three i-genes BTN3A2, CD2, and TRBC1 and the p-gene MMP11) were significantly associated with distant metastasis-free survival (DMFS). A new prognostic model for HR-/HER2+ breast cancer based on the expression of MMP11 and CD2 was developed and the DMFS for patients in the high-risk group according to our model was significantly lower than that for those in the low-risk group. Multivariate analyses revealed that our risk score is an independent prognostic factor for DMFS. Moreover, C-index showed that our risk score has a superior prognostic performance to traditional clinicopathological factors. Conclusions Our new prognostic model for HR-/HER2+ breast cancer provides more accurate information on the risk of distant metastasis than traditional clinical prognostic factors and may be used to identify patients with a good prognosis in this aggressive subtype of breast cancer.
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