The DOI matches its Crossref record; 173 of the 173 references it cites were found in a registry or an index.
Squamous Cell Cancers: A Unified Perspective on Biology and Genetics
Open accessAbstract
SUMMARY Squamous cell carcinomas (SCCs) represent the most frequent human solid tumors and a major cause of cancer mortality. These highly heterogeneous tumors arise from closely interconnected epithelial cell populations with intrinsic self-renewal potential inversely related to the stratified differentiation program. SCCs can also originate from simple or pseudo-stratified epithelia through activation of quiescent cells and/or a switch in cell fate determination. Here, we focus on specific determinants implicated in the development of SCCs by recent large-scale genomic, genetic and epigenetic studies and complementary functional analysis. This evidence indicates that SCCs from various body sites, while clinically treated as separate entities, have common determinants, pointing to a unified perspective of the disease and potential new avenues for prevention and treatment.
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1 retracted
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IL-6 Mediates Cross-Talk between Tumor Cells and Activated Fibroblasts in the Tumor Microenvironment
Karakasheva, T. A., Lin, E. W., Tang, Q., Qiao, E., Waldron, T. J., Soni, M., Klein-Szanto, A. J., Sahu, V., Basu, D., Ohashi, S., et al. (2018) · Cancer Research · doi:10.1158/0008-5472.can-17-2268 · Cited by 250
Self-citation
Metadata
- Authors
- Dotto, G. P., & Rustgi, A. K.
- Venue
- Cancer Cell
- Publisher
- Elsevier BV
- Published
- 2016-05
- Volume
- 29
- Issue
- 5
- Pages
- 622-637
- ISSN
- 1535-6108 (ISSN-L)
- OpenAlex
- W2346530374
- Cited by
- 319
- References
- 173
- FWCI
- 21.60
- Type
- journal article
- Language
- en
- Open access
- bronze
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.
