The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
Tumor Cell Dissemination: Emerging Biological Insights from Animal Models and Cancer Patients
Open accessAbstract
Circulating tumor cells (CTCs) and disseminated tumor cells (DTCs) are increasingly recognized for their potential utility in disease monitoring and therapeutic targeting. The clinical application of CTC/DTC requires better understanding of the biological mechanisms behind tumor dissemination, the survival of DTCs, and their activation to aggressive growth from dormancy. Recent research using animal models of DTCs and CTCs have provided novel insights into these processes. Here we discuss these findings in the context of results obtained from the clinical analyses of CTCs and DTCs, which demonstrates that the animal models mimic in many aspects the complex situation in patients.
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Citations
Cites
1 retracted
Lysyl oxidase is essential for hypoxia-induced metastasis
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Cited by
Emerging Biological Principles of Metastasis
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Metastatic colonization by circulating tumour cells
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Clinical Applications of Circulating Tumor Cells and Circulating Tumor DNA as Liquid Biopsy
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Self-citationChallenges in circulating tumour cell research
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Self-citationClinical relevance of circulating cell-free microRNAs in cancer
Schwarzenbach, H., Nishida, N., Calin, G. A., & Pantel, K. (2014) · Nature Reviews Clinical Oncology · doi:10.1038/nrclinonc.2014.5 · Cited by 969
Self-citation
Metadata
- Authors
- Kang, Y., & Pantel, K.
- Venue
- Cancer Cell
- Publisher
- Elsevier BV
- Published
- 2013-05
- Volume
- 23
- Issue
- 5
- Pages
- 573-581
- ISSN
- 1535-6108 (ISSN-L)
- OpenAlex
- W2054017641
- Cited by
- 421
- References
- 8
- FWCI
- 23.56
- Type
- journal article
- Language
- en
- Open access
- bronze
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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.
