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Cited by 2,452

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

Triple-negative breast cancer molecular subtyping and treatment progress

Open access
Yin, Li, Duan, Jiang-Jie, Bian, Xiu-Wu, Yu, Shi-cang·2020·Breast Cancer Research

Abstract

Triple-negative breast cancer (TNBC), a specific subtype of breast cancer that does not express estrogen receptor (ER), progesterone receptor (PR), or human epidermal growth factor receptor 2 (HER-2), has clinical features that include high invasiveness, high metastatic potential, proneness to relapse, and poor prognosis. Because TNBC tumors lack ER, PR, and HER2 expression, they are not sensitive to endocrine therapy or HER2 treatment, and standardized TNBC treatment regimens are still lacking. Therefore, development of new TNBC treatment strategies has become an urgent clinical need. By summarizing existing treatment regimens, therapeutic drugs, and their efficacy for different TNBC subtypes and reviewing some new preclinical studies and targeted treatment regimens for TNBC, this paper aims to provide new ideas for TNBC treatment.

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Metadata

Authors
Yin, L., Duan, J.-J., Bian, X.-W., & Yu, S.-C.
Venue
Breast Cancer Research
Published
2020-06-09
Volume
22
Issue
1
Pages
61-61
ISSN
  • 1465-5411 (ISSN-L)
  • 1465-542X
OpenAlex
W3033869790
Cited by
2,452
References
6
FWCI
78.74
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Triple-negative breast cancer molecular subtyping and treatment progress. https://app.cochat.ai/papers/10.1186/s13058-020-01296-5
The paper
Yin, L., Duan, J.-J., Bian, X.-W., & Yu, S.-C. (2020). Triple-negative breast cancer molecular subtyping and treatment progress. Breast Cancer Research. https://doi.org/10.1186/s13058-020-01296-5

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.