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Obesity-related proteins score as a potential marker of breast cancer risk

There is strong evidence to suggest that obesity-related proteins play a key role in pathways that are related to breast cancer. In this study, we aimed to establish a robust obesity-related protein score (ORPS) that could be used to assess breast cancer risk. Based on evidence from high-quality sys...

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Bibliographic Details
Published in:Scientific reports 2021-04, Vol.11 (1), p.8230-8230, Article 8230
Main Authors: Diao, Sha, Wu, Xueyao, Zhang, Xiaofan, Hao, Yu, Xu, Bin, Li, Xu, Tian, Lulu, Miao, Yunqi, Zhao, Xunying, Ye, Feng, Li, Jiayuan
Format: Article
Language:English
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Summary:There is strong evidence to suggest that obesity-related proteins play a key role in pathways that are related to breast cancer. In this study, we aimed to establish a robust obesity-related protein score (ORPS) that could be used to assess breast cancer risk. Based on evidence from high-quality systematic reviews and population studies, we selected nine such proteins that are stable in vitro, and measured their circulating concentrations by ELISA in a case–control study conducted in Chengdu, Sichuan, China, with 279 breast cancer cases and 260 healthy controls. Two obesity-related protein scores (ORPS) were calculated using a three-step method, with linear-weighted summation, and the one with a larger area under the curve was chosen for further evaluation. As a result, ORPS (PS 5pre or PS 4post ) was positively correlated with breast cancer risk (premenopausal: OR ≤63 VS >63 3.696, 95% CI 2.025–6.747; postmenopausal: OR ≤38 VS >38 7.100, 95% CI 3.134–16.084), and represented a better risk predictor among obese women compared to non-obese in pre- and postmenopausal women. Among different molecular subtypes, ORPS was positively correlated with Luminal breast cancer, with additionally positive association with triple-negative breast cancer in premenopausal women. The ORPS might be a potential marker of breast cancer risk among Chinese women.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-021-87583-3