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• W4220996923 abstract "Future Medicinal ChemistryVol. 14, No. 8 EditorialCombining EGFR inhibitors with SHP2 or LSD1 inhibitors to overcome multidrug resistance in cancerHuiqing Zhang, Xinyu Yang, Yihui Song & Bin YuHuiqing ZhangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, ChinaSearch for more papers by this author, Xinyu YangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, ChinaSearch for more papers by this author, Yihui Song *Author for correspondence: Tel.: +86 0371 6778 1908; E-mail Address: songyihui@zzu.edu.cnhttps://orcid.org/0000-0001-7922-1209School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, ChinaSearch for more papers by this author & Bin Yu **Author for correspondence: E-mail Address: zzuyubin@hotmail.comhttps://orcid.org/0000-0002-7207-643XSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, ChinaSearch for more papers by this authorPublished Online:30 Mar 2022https://doi.org/10.4155/fmc-2021-0326AboutSectionsView ArticleView Full TextPDF/EPUB ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareShare onFacebookTwitterLinkedInReddit View articleKeywords: combination therapyEGFRLSD1multidrug resistanceSHP2References1. 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Chem. 84, 164–169 (2019).Crossref, Medline, CAS, Google Scholar20. Zheng M, Huo J, Gu X et al. Rational design and synthesis of novel dual PROTACs for simultaneous degradation of EGFR and PARP. J. Med. Chem. 64(11), 7839–7852 (2021).Crossref, Medline, CAS, Google ScholarFiguresReferencesRelatedDetailsCited ByTargeting SHP2 for Cancer Treatment: Advances and Prospects4 January 2023Harnessing the cyclization strategy for new drug discoveryActa Pharmaceutica Sinica B, Vol. 12, No. 12 Vol. 14, No. 8 Follow us on social media for the latest updates Metrics Downloaded 207 times History Received 20 November 2021 Accepted 19 January 2022 Published online 30 March 2022 Published in print April 2022 Information© 2022 Newlands PressKeywordscombination therapyEGFRLSD1multidrug resistanceSHP2Financial & competing interests disclosureThis work is supported by the National Natural Science Foundation of China (no. 31900875 and 81973177). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.No writing assistance was utilized in the production of this manuscript.PDF download" @default.
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