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 accessAbstract
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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Ogier du Terrail, J., Leopold, A., Joly, C., Béguier, C., Andreux, M., Maussion, C., Schmauch, B., Tramel, E. W., Bendjebbar, E., Zaslavskiy, M., et al. (2023) · Nature Medicine · doi:10.1038/s41591-022-02155-w · Cited by 217
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Sarkar, R., Biswas, S., Ghosh, R., Samanta, P., Pakhira, S., Mondal, M., Dutta Gupta, Y., Bhandary, S., Saha, P., Bhowmik, A., et al. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02518-0 · Cited by 69
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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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.