{"id":10378,"date":"2022-10-06T00:04:52","date_gmt":"2022-10-05T16:04:52","guid":{"rendered":"https:\/\/newsletter.sinica.edu.tw/en\/?p=10378"},"modified":"2024-03-13T09:19:04","modified_gmt":"2024-03-13T01:19:04","slug":"phyto-sesquiterpene-lactones-det-and-detd-35-induce-ferroptosis-in-vemurafenib-sensitive-and-resistant-melanoma-via-gpx4-inhibition-and-metabolic-reprogramming","status":"publish","type":"post","link":"https:\/\/newsletter.sinica.edu.tw/en\/10378\/","title":{"rendered":"Phyto-sesquiterpene lactones DET and DETD-35 induce ferroptosis in vemurafenib sensitive and resistant melanoma via GPX4 inhibition and metabolic reprogramming"},"content":{"rendered":"
Melanoma is the most life-threatening form of skin cancer. More than 50% of melanoma patients carry BRAFV600E<\/sup> mutation, but most patients develop resistance, side effects, and relapse after treatment with BRAFV600E<\/sup> inhibitor drugs such as vemurafenib. Dr. Lie-Fen Shyur\u2019s team at the Agricultural Biotechnology Research Center discovered that sesquiterpene lactone deoxyelephantopin (DET) and its structurally modified derivative DETD-35 are novel GPX4 inhibitors and ferroptosis inducers through which vemurafenib induced abnormal primary and lipid metabolisms in resistant melanoma were reversed; in turn, vemurafenib drug sensitivity to resistant melanoma was enhanced. DET and DETD-35 show great potential as BRAFV600E<\/sup> inhibitor drug adjuvants against melanoma. This study was published in Pharmacological Research<\/em>.<\/p>\n For further information:
\nhttps:\/\/abrc.sinica.edu.tw\/en\/view.php?aid=6268&wid=2<\/a><\/p>\n