Paper · 42809705
Auranofin Potentiates Cisplatin Response in the Setting of Context-Dependent NOTCH-Associated Signaling States in Endometrial Cancer.
Lake RJ and 8 others. Cancer Res Commun, 2026.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. Auranofin Potentiates Cisplatin Response in the Setting of Context-Dependent NOTCH-Associated Signaling States in Endometrial Cancer. Papers, record 42809705. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/42809705
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Auranofin Potentiates Cisplatin Response in the Setting of Context-Dependent NOTCH-Associated Signaling States in Endometrial Cancer.
- Journal
- Cancer Res Commun
- Year
- 2026
- Publication types
- Journal Article
- Revised in PubMed
- 2026-11-06
Source PubMed
Topics16
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Endometrial Neoplasms | Major topic |
| Auranofin | Major topic |
| Cisplatin | Major topic |
| Receptors, Notch | Major topic |
| Receptor, Notch3 | Major topic |
| Antineoplastic Combined Chemotherapy Protocols | Major topic |
| Female | |
| Humans | |
| Animals | |
| Signal Transduction | |
| Mice | |
| Cell Line, Tumor | |
| Drug Synergism | |
| Xenograft Model Antitumor Assays | |
| Drug Resistance, Neoplasm | |
| Gene Expression Regulation, Neoplastic |
Source PubMed
Grants7
Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.
| Grant, as the record writes it | Agency | Country | NIH project | Stated by | Source |
|---|---|---|---|---|---|
| 21CA286210 | National Cancer Institute (NCI) | PubMed | PubMed | ||
| P30CA118100 | Center for Cancer Research (CCR) | P30CA118100 | PubMed | NIH RePORTER | |
| R21 CA286210 | NCI NIH HHS | United States | R21CA286210 | PubMed | NIH RePORTER |
| CA210610 | U.S. Department of War (DOW) | PubMed | PubMed | ||
| OC230061 | U.S. Department of War (DOW) | PubMed | PubMed | ||
| P50CA265793 | National Cancer Institute (NCI) | P50CA265793 | PubMed | NIH RePORTER | |
| P30 CA118100 | NCI NIH HHS | United States | P30CA118100 | PubMed | NIH RePORTER |
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
PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.
None in this release.
References44
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 | 40,985,842 | Auranofin Synergizes with Cisplatin in Reducing Tumor Burden of NOTCH-Dependent Ovarian Cancer. | Cancer Res Commun | 2025 | https://conductscience.org/library/papers/40985842 | PubMed |
| 2 | 38,269,508 | Auranofin sensitizes breast cancer cells to paclitaxel mediated cell death via regulating FOXO3/Nrf2/Keap1 signaling pathway. | Cell Biochem Funct | 2024 | https://conductscience.org/library/papers/38269508 | PubMed |
| 3 | 37,712,875 | A Phase I Study of the Pan-Notch Inhibitor CB-103 for Patients with Advanced Adenoid Cystic Carcinoma and Other Tumors. | Cancer Res Commun | 2023 | https://conductscience.org/library/papers/37712875 | PubMed |
| 4 | 24,298,019 | Notch-Nrf2 axis: regulation of Nrf2 gene expression and cytoprotection by notch signaling. | Mol Cell Biol | 2014 | https://conductscience.org/library/papers/24298019 | PubMed |
| 5 | 17,525,745 | Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes. | Oncogene | 2007 | https://conductscience.org/library/papers/17525745 | PubMed |
| 6 | 37,165,578 | FGFR2 mutations promote endometrial cancer progression through dual engagement of EGFR and Notch signalling pathways. | Clin Transl Med | 2023 | https://conductscience.org/library/papers/37165578 | PubMed |
| 7 | 33,284,507 | Gamma Secretase Inhibitors in Cancer: A Current Perspective on Clinical Performance. | Oncologist | 2021 | https://conductscience.org/library/papers/33284507 | PubMed |
| 8 | 41,154,495 | The Redox Paradox: Cancer's Double-Edged Sword for Malignancy and Therapy. | Antioxidants (Basel) | 2025 | https://conductscience.org/library/papers/41154495 | PubMed |
| 9 | 40,052,152 | Notch signaling in cancers: mechanism and potential therapy. | Front Cell Dev Biol | 2025 | https://conductscience.org/library/papers/40052152 | PubMed |
| 10 | 23,019,585 | Targeting Notch, a key pathway for ovarian cancer stem cells, sensitizes tumors to platinum therapy. | Proc Natl Acad Sci U S A | 2012 | https://conductscience.org/library/papers/23019585 | PubMed |
1 to 10 of 44
See all 44 referencesCited by0
The papers in our copy of PubMed whose reference list names this one, newest first.
None in this release.
Genes5
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 |
|---|---|---|---|---|
| HES1 | 3,280 | PubTator's text mining | https://conductscience.org/library/genes/3280 | NCBI Gene |
| HES4 | 57,801 | PubTator's text mining | https://conductscience.org/library/genes/57801 | NCBI Gene |
| NOTCH3 | 4,854 | PubTator's text mining | https://conductscience.org/library/genes/4854 | NCBI Gene |
| PRDX5 | 25,824 | PubTator's text mining | https://conductscience.org/library/genes/25824 | NCBI Gene |
| RBPJ | 3,516 | PubTator's text mining | https://conductscience.org/library/genes/3516 | 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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