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Exome Sequencing of Plasma DNA Portrays the Mutation Landscape of Colorectal Cancer and Discovers Mutated VEGFR2 Receptors as Modulators of Antiangiogenic Therapies.
- Source :
-
Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2018 Aug 01; Vol. 24 (15), pp. 3550-3559. Date of Electronic Publication: 2018 Mar 27. - Publication Year :
- 2018
-
Abstract
- Purpose: Despite the wide use of antiangiogenic drugs in the clinical setting, predictive biomarkers of response to these drugs are still unknown. Experimental Design: We applied whole-exome sequencing of matched germline and basal plasma cell-free DNA samples (WES-cfDNA) on a RAS/BRAF/PIK3CA wild-type metastatic colorectal cancer patient with primary resistance to standard treatment regimens, including inhibitors to the VEGF:VEGFR2 pathway. We performed extensive functional experiments, including ectopic expression of VEGFR2 mutants in different cell lines, kinase and drug sensitivity assays, and cell- and patient-derived xenografts. Results: WES-cfDNA yielded a 77% concordance rate with tumor exome sequencing and enabled the identification of the KDR /VEGFR2 L840F clonal, somatic mutation as the cause of therapy refractoriness in our patient. In addition, we found that 1% to 3% of samples from cancer sequencing projects harbor KDR somatic mutations located in protein residues frequently mutated in other cancer-relevant kinases, such as EGFR, ABL1, and ALK. Our in vitro and in vivo functional assays confirmed that L840F causes strong resistance to antiangiogenic drugs, whereas the KDR hot-spot mutant R1032Q confers sensitivity to strong VEGFR2 inhibitors. Moreover, we showed that the D717V, G800D, G800R, L840F, G843D, S925F, R1022Q, R1032Q, and S1100F VEGFR2 mutants promote tumor growth in mice. Conclusions: Our study supports WES-cfDNA as a powerful platform for portraying the somatic mutation landscape of cancer and discovery of new resistance mechanisms to cancer therapies. Importantly, we discovered that VEGFR2 is somatically mutated across tumor types and that VEGFR2 mutants can be oncogenic and control sensitivity/resistance to antiangiogenic drugs. Clin Cancer Res; 24(15); 3550-9. ©2018 AACR .<br /> (©2018 American Association for Cancer Research.)
- Subjects :
- Anaplastic Lymphoma Kinase genetics
Angiogenesis Inhibitors adverse effects
Animals
Biomarkers, Tumor genetics
Cell Line, Tumor
Cell Proliferation genetics
Cell-Free Nucleic Acids blood
Cell-Free Nucleic Acids genetics
Class I Phosphatidylinositol 3-Kinases genetics
Colorectal Neoplasms blood
Colorectal Neoplasms drug therapy
Colorectal Neoplasms pathology
ErbB Receptors genetics
Exome genetics
Female
Heterografts
Humans
Mice
Mutation
Neovascularization, Pathologic blood
Neovascularization, Pathologic drug therapy
Neovascularization, Pathologic pathology
Protein Conformation drug effects
Proto-Oncogene Proteins c-abl genetics
Vascular Endothelial Growth Factor A genetics
Vascular Endothelial Growth Factor Receptor-2 blood
Vascular Endothelial Growth Factor Receptor-2 chemistry
Exome Sequencing
Angiogenesis Inhibitors administration & dosage
Colorectal Neoplasms genetics
Neovascularization, Pathologic genetics
Vascular Endothelial Growth Factor Receptor-2 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1557-3265
- Volume :
- 24
- Issue :
- 15
- Database :
- MEDLINE
- Journal :
- Clinical cancer research : an official journal of the American Association for Cancer Research
- Publication Type :
- Academic Journal
- Accession number :
- 29588308
- Full Text :
- https://doi.org/10.1158/1078-0432.CCR-18-0103