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Validating Stat3 in cancer therapy
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“This is especially the case in over 95% of patients with head and neck squamous cell carcinoma (HNSCC) and 57.4% of patients with colorectal cancer (CRC) (3–5).”
From Small-molecule PROTAC mediates targeted protein degradation to treat STAT3-dependent epithelial cancer (2022) · cites this paper as [5]
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Metadata
- Authors
- Darnell, J. E.
- Affiliations
- Rockefeller University (US)
- Corresponding author
- Darnell, James E
- Venue
- Nature Medicine
- Published
- 2005-06
- Volume
- 11
- Issue
- 6
- Pages
- 595-596
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- OpenAlex
- W1977532256
- Cited by
- 307
- References
- 15
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 11 · 2023: 3 · 2022: 8 · 2021: 7 · 2020: 11 · 2019: 8 · 2018: 21 · 2017: 14 · 2016: 15 · 2015: 9 · 2014: 27 · 2013: 30 · 2012: 17
- FWCI
- 10.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Mechanisms and Therapy
- Keywords
- STAT3, transcription factors, cancer therapy, STAT3 inhibitor, therapeutic target, in vivo validation, anticancer agents
- MeSH terms
- Animals, Antineoplastic Agents, DNA-Binding Proteins, Humans, Neoplasm Proteins, Neoplasms, Trans-Activators, STAT3 Transcription Factor
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