Paper · 41476672
The Landscape of Potential Targeted Treatments and Chemotherapy Efficacy Biomarkers for TNBC.
Kang Y and 4 others. Breast Cancer (Dove Med Press), 2025. Cited by 0 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. The Landscape of Potential Targeted Treatments and Chemotherapy Efficacy Biomarkers for TNBC. Papers, record 41476672. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/41476672
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Paper
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- Title
- The Landscape of Potential Targeted Treatments and Chemotherapy Efficacy Biomarkers for TNBC.
- PubMed
Topics0
NLM's MeSH indexing of the paper, its major topics first.
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Grants0
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Trials0
The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.
None in this release.
Comments and corrections0
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None in this release.
References227
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 34,692,516 | Atractylenolide-I Sensitizes Triple-Negative Breast Cancer Cells to Paclitaxel by Blocking CTGF Expression and Fibroblast Activation. | Front Oncol | 2021 | https://conductscience.org/library/papers/34692516 | PubMed |
| 2 | 30,679,171 | Insights into Molecular Classifications of Triple-Negative Breast Cancer: Improving Patient Selection for Treatment. | Cancer Discov | 2019 | https://conductscience.org/library/papers/30679171 | PubMed |
| 3 | 30,798,356 | T cell-redirecting bispecific antibodies in cancer immunotherapy: recent advances. | J Cancer Res Clin Oncol | 2019 | https://conductscience.org/library/papers/30798356 | PubMed |
| 4 | 21,884,205 | Epidermal growth factor receptor gene amplification and protein overexpression in basal-like carcinoma of the breast. | Histopathology | 2011 | https://conductscience.org/library/papers/21884205 | PubMed |
| 5 | 36,568,247 | Ferroptosis and triple-negative breast cancer: Potential therapeutic targets. | Front Oncol | 2022 | https://conductscience.org/library/papers/36568247 | PubMed |
| 6 | 35,414,060 | Identification of a novel mechanism for reversal of doxorubicin-induced chemotherapy resistance by TXNIP in triple-negative breast cancer via promoting reactive oxygen-mediated DNA damage. | Cell Death Dis | 2022 | https://conductscience.org/library/papers/35414060 | PubMed |
| 7 | 20,164,688 | Triple-negative breast cancer: role of antiangiogenic agents. | Cancer J | 2010 | https://conductscience.org/library/papers/20164688 | PubMed |
| 8 | 31,927,455 | Triple negative breast cancer: A thorough review of biomarkers. | Crit Rev Oncol Hematol | 2020 | https://conductscience.org/library/papers/31927455 | PubMed |
| 9 | 33,352,844 | The Emerging Therapeutic Landscape of ALK Inhibitors in Non-Small Cell Lung Cancer. | Pharmaceuticals (Basel) | 2020 | https://conductscience.org/library/papers/33352844 | PubMed |
| 10 | 22,258,607 | The DNA damage response and cancer therapy. | Nature | 2012 | https://conductscience.org/library/papers/22258607 | PubMed |
1 to 10 of 227
See all 227 referencesCited by2
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 0 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 42,870,830 | MIF-mediated intercellular crosstalk drives antigen-presenting-like cancer-associated fibroblast differentiation in triple-negative breast cancer via TGF-β signaling. | Transl Cancer Res | 2026 | https://conductscience.org/library/papers/42870830 | PubMed |
| 42,858,231 | RecurIndex-derived molecular features associated with total pathological complete response in triple-negative breast cancer: An exploratory prospective cohort study with single-cell transcriptomic contextualization. | Cancer Biol Ther | 2026 | https://conductscience.org/library/papers/42858231 | PubMed |
Genes4
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
| Gene | NCBI Gene ID | Linked by | In Genes | Source |
|---|---|---|---|---|
| EGFR | 1,956 | PubTator's text mining | https://conductscience.org/library/genes/1956 | NCBI Gene |
| ERBB2 | 2,064 | PubTator's text mining | https://conductscience.org/library/genes/2064 | NCBI Gene |
| ESR1 | 2,099 | PubTator's text mining | https://conductscience.org/library/genes/2099 | NCBI Gene |
| PGR | 5,241 | PubTator's text mining | https://conductscience.org/library/genes/5241 | NCBI Gene |
Drugs0
The drugs whose trials, in the Pipelines release, list the paper.
None in this release.
Data0
The data bank entries PubMed's record names. Trial numbers are under Trials.
None in this release.
Data dates
The date of each source this release read.
- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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