| Literature DB >> 31597506 |
Tao Wang1, Shunqiang Xie1, Rongtuan Luo1, Lianguo Shi2, Peide Bai1, Xuegang Wang1, Rui Wan1, Jiang Deng1, Zhun Wu1, Wei Li1, Wen Xiao1, Yongfeng Wang1, Bin Chen1, Kaiyan Zhang1, Jinchun Xing1.
Abstract
People who suffers renal angiomyolipoma (AML) has a low quality of life. It is widely known that genetic factors including TSC2 mutation contribute to certain populations of renal AML-bearing patients. In this study, we are the first to identify novel TSC2 mutations in one Chinese renal epithelioid AML patient: c.2652C>A; c.2688G>A based on sequencing result from biopsy tissue. These two somatic mutations cause a translational stop of TSC2, which leads to mTORC1 activation. Given the fact that activation of mTORC1 ensures cell growth and survival, we applied its inhibitor, FDA-approved everolimus, to this woman. After months of treatment with everolimus, Computer-Tomography (CT) scan results showed that everolimus successfully reduced tumor growth and distal metastasis and achieved partial response (PR) to everolimu according to Response Evaluation Criteria in Solid Tumors (RECIST version 1.1). Further Blood Routine Examination results showed the concentration of red cell mass, hemoglobin, white blood cell (WBC), platelets and hematocrit (HCT) significantly returned to normal levels indicating patients with these two TSC2 mutations could be effectively treated by everolimus.Entities:
Keywords: Renal epithelioid angiomyolipoma; TSC2 mutation; everolimus; mTORC1
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Year: 2019 PMID: 31597506 PMCID: PMC7012169 DOI: 10.1080/15384047.2019.1665955
Source DB: PubMed Journal: Cancer Biol Ther ISSN: 1538-4047 Impact factor: 4.742