题名 | KRAS mutation-driven angiopoietin 2 bestows anti-VEGF resistance in epithelial carcinomas |
作者 | |
发表日期 | 2023-07-18 |
发表期刊 | Proceedings of the National Academy of Sciences of the United States of America 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Journal Article ; Research Support, Non-U.S. Gov't |
关键词 | ANG2 Ras mutation VEGF cancer drug resistance |
其他关键词 | ENDOTHELIAL GROWTH-FACTOR ; TUMOR-GROWTH ; HUMAN CANCER ; ANTIANGIOGENIC THERAPY ; DISEASE PROGRESSION ; MONOCLONAL-ANTIBODY ; RAS MUTATIONS ; PHASE-I ; ANGIOGENESIS ; EXPRESSION |
摘要 | Defining reliable surrogate markers and overcoming drug resistance are the most challenging issues for improving therapeutic outcomes of antiangiogenic drugs (AADs) in cancer patients. At the time of this writing, no biomarkers are clinically available to predict AAD therapeutic benefits and drug resistance. Here, we uncovered a unique mechanism of AAD resistance in epithelial carcinomas with KRAS mutations that targeted angiopoietin 2 (ANG2) to circumvent antivascular endothelial growth factor (anti-VEGF) responses. Mechanistically, KRAS mutations up-regulated the FOXC2 transcription factor that directly elevated ANG2 expression at the transcriptional level. ANG2 bestowed anti-VEGF resistance as an alternative pathway to augment VEGF-independent tumor angiogenesis. Most colorectal and pancreatic cancers with KRAS mutations were intrinsically resistant to monotherapies of anti-VEGF or anti-ANG2 drugs. However, combination therapy with anti-VEGF and anti-ANG2 drugs produced synergistic and potent anticancer effects in KRAS-mutated cancers. Together, these data demonstrate that KRAS mutations in tumors serve as a predictive marker for anti-VEGF resistance and are susceptible to combination therapy with anti-VEGF and anti-ANG2 drugs. |
资助项目 | European Research Council[250021];National Key R&D Program of China[2020YFC0846600]; |
出版者 | NATL ACAD SCIENCES |
ISSN | 0027-8424 |
EISSN | 1091-6490 |
卷号 | 120期号:29 |
DOI | 10.1073/pnas.2303740120 |
页数 | 12 |
WOS类目 | Multidisciplinary Sciences |
WOS研究方向 | Science & Technology - Other Topics |
WOS记录号 | WOS:001262308700003 |
收录类别 | PUBMED ; SCOPUS ; SCIE |
URL | 查看原文 |
PubMed ID | 37428914 |
SCOPUSEID | 2-s2.0-85164274574 |
自科自定义期刊分类 | T3(A)类 |
通讯作者地址 | [Cao, Yihai]Department of Microbiology,Tumor and Cell Biology,Karolinska Institute,Stockholm,171 65,Sweden |
Scopus学科分类 | Multidisciplinary |
TOP期刊 | TOP期刊 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/181682 |
专题 | 药学院(分析测试中心) |
通讯作者 | Cao, Yihai |
作者单位 | 1.Department of Microbiology,Tumor and Cell Biology,Karolinska Institute,Stockholm,171 65,Sweden; 2.Department of Gastroenterology,Sir Run Run Shaw Hospital,Zhejiang University School of Medicine,Zhejiang,Hangzhou,310016,China; 3.School of Pharmacology,Binzhou Medical University,Shandong,Yantai,264003,China; 4.Oujiang Laboratory,Zhejiang Lab for Regenerative Medicine,Vison and Brain Health,School of Pharmaceutical Science,Wenzhou Medical University,Wenzhou,325024,China; 5.Department of Pharmacy,Zhejiang Provincial People’s Hospital,People’s Hospital of Hangzhou Medical College,Hangzhou,310053,China; 6.Department of Cellular and Genetic Medicine,School of Basic Medical Sciences,Fudan University,Shanghai,200032,China; 7.Department of Head,Neck and Thyroid Surgery,Zhejiang Provincial People’s Hospital,People’s Hospital of Hangzhou Medical College,Hangzhou,31003,China |
推荐引用方式 GB/T 7714 | Hosaka, Kayoko,Andersson, Patrik,Wu, Jieyu,et al. KRAS mutation-driven angiopoietin 2 bestows anti-VEGF resistance in epithelial carcinomas[J]. Proceedings of the National Academy of Sciences of the United States of America,2023,120(29). |
APA | Hosaka, Kayoko., Andersson, Patrik., Wu, Jieyu., He, Xingkang., Du, Qiqiao., ... & Cao, Yihai. (2023). KRAS mutation-driven angiopoietin 2 bestows anti-VEGF resistance in epithelial carcinomas. Proceedings of the National Academy of Sciences of the United States of America, 120(29). |
MLA | Hosaka, Kayoko,et al."KRAS mutation-driven angiopoietin 2 bestows anti-VEGF resistance in epithelial carcinomas".Proceedings of the National Academy of Sciences of the United States of America 120.29(2023). |
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