Literature DB >> 33572269

Cell Line Models for Acquired Resistance to First-Line Osimertinib in Lung Cancers-Applications and Limitations.

Shuta Ohara1, Kenichi Suda1, Tetsuya Mitsudomi1.   

Abstract

Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are first-line drugs for lung cancers with activating EGFR mutations. Although first- and second-generation EGFR-TKIs were standard first-line treatments, acquired resistance (AR) to these drugs is almost inevitable. Cell line models have been widely used to explore the molecular mechanisms of AR to first- and second-generation EGFR-TKIs. Many research groups, including ours, have established AR cell lines that harbor the EGFR T790M secondary mutation, MET gene amplification, or epithelial-mesenchymal transition (EMT) features, which are all found in clinical specimens obtained from TKI-refractory lesions. Currently, many oncologists prescribe osimertinib, a third-generation EGFR-TKI that can overcome T790M-mediated resistance, as a first-line TKI. Although few clinical data are available about AR mechanisms that arise when osimertinib is used as a first-line therapy, many research groups have established cell lines with AR to osimertinib and have reported on their AR mechanisms. In this review, we summarize the findings on AR mechanisms against first-line osimertinib obtained from analyses of cell line models.

Entities:  

Keywords:  EGFR mutation; acquired resistance; bypass pathway; cell line models; epithelial to mesenchymal transition (EMT); non-small-cell lung cancer; osimertinib

Mesh:

Substances:

Year:  2021        PMID: 33572269      PMCID: PMC7915563          DOI: 10.3390/cells10020354

Source DB:  PubMed          Journal:  Cells        ISSN: 2073-4409            Impact factor:   6.600


  94 in total

1.  CA916798 regulates multidrug resistance of lung cancer cells.

Authors:  Hai-Jing Wang; He-Ping Yang; Xiang-Dong Zhou; Xiao-Tian Dai; Yong-Feng Chen; Wei Xiong
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2.  Acquired resistance to EGFR tyrosine kinase inhibitors is mediated by the reactivation of STC2/JUN/AXL signaling in lung cancer.

Authors:  Yi-Nan Liu; Meng-Feng Tsai; Shang-Gin Wu; Tzu-Hua Chang; Tzu-Hsiu Tsai; Chien-Hung Gow; Yih-Leong Chang; Jin-Yuan Shih
Journal:  Int J Cancer       Date:  2019-06-25       Impact factor: 7.396

3.  Epigenetics and miRNA as predictive markers and targets for lung cancer chemotherapy.

Authors:  Raafat A El-Awady; Fatema Hersi; Hala Al-Tunaiji; Ekram M Saleh; Abdel-Hady A Abdel-Wahab; Amer Al Homssi; Mousa Suhail; Ahmed El-Serafi; Taleb Al-Tel
Journal:  Cancer Biol Ther       Date:  2015       Impact factor: 4.742

4.  A YAP/FOXM1 axis mediates EMT-associated EGFR inhibitor resistance and increased expression of spindle assembly checkpoint components.

Authors:  Monique B Nilsson; Huiying Sun; Jacqulyne Robichaux; Matthias Pfeifer; Ultan McDermott; Jon Travers; Lixia Diao; Yuanxin Xi; Pan Tong; Li Shen; Mia Hofstad; Masanori Kawakami; Xiuning Le; Xi Liu; Youhong Fan; Alissa Poteete; Limei Hu; Marcelo V Negrao; Hai Tran; Ethan Dmitrovsky; David Peng; Don L Gibbons; Jing Wang; John V Heymach
Journal:  Sci Transl Med       Date:  2020-09-02       Impact factor: 17.956

5.  Hsp90 inhibitors enhance the antitumoral effect of osimertinib in parental and osimertinib-resistant non-small cell lung cancer cell lines.

Authors:  Jordi Codony-Servat; Santiago Viteri; Carles Codony-Servat; Masaoki Ito; Jillian Willhelmina Paulina Bracht; Jordi Berenguer; Imane Chaib; Miguel Angel Molina-Vila; Niki Karachaliou; Rafael Rosell
Journal:  Transl Lung Cancer Res       Date:  2019-08

6.  Acquired BRAF V600E Mutation Mediated Resistance to Osimertinib and Responded to Osimertinib, Dabrafenib, and Trametinib Combination Therapy.

Authors:  Yihua Huang; Jiadi Gan; Kunbin Guo; Yangyang Deng; Wenfeng Fang
Journal:  J Thorac Oncol       Date:  2019-10       Impact factor: 15.609

7.  AXL confers intrinsic resistance to osimertinib and advances the emergence of tolerant cells.

Authors:  Hirokazu Taniguchi; Tadaaki Yamada; Rong Wang; Keiko Tanimura; Yuta Adachi; Akihiro Nishiyama; Azusa Tanimoto; Shinji Takeuchi; Luiz H Araujo; Mariana Boroni; Akihiro Yoshimura; Shinsuke Shiotsu; Isao Matsumoto; Satoshi Watanabe; Toshiaki Kikuchi; Satoru Miura; Hiroshi Tanaka; Takeshi Kitazaki; Hiroyuki Yamaguchi; Hiroshi Mukae; Junji Uchino; Hisanori Uehara; Koichi Takayama; Seiji Yano
Journal:  Nat Commun       Date:  2019-01-16       Impact factor: 14.919

8.  Landscape of EGFR-Dependent and -Independent Resistance Mechanisms to Osimertinib and Continuation Therapy Beyond Progression in EGFR-Mutant NSCLC.

Authors:  Xiuning Le; Sonam Puri; Marcelo V Negrao; Monique B Nilsson; Jacqulyne Robichaux; Theresa Boyle; J Kevin Hicks; Katherine L Lovinger; Emily Roarty; Waree Rinsurongkawong; Ming Tang; Huiying Sun; Yasir Elamin; Lara C Lacerda; Jeff Lewis; Jack A Roth; Stephen G Swisher; J Jack Lee; William N William; Bonnie S Glisson; Jianjun Zhang; Vassiliki A Papadimitrakopoulou; Jhanelle E Gray; John V Heymach
Journal:  Clin Cancer Res       Date:  2018-09-18       Impact factor: 12.531

9.  Combined osimertinib, dabrafenib and trametinib treatment for advanced non-small-cell lung cancer patients with an osimertinib-induced BRAF V600E mutation.

Authors:  Pei Meng; Bart Koopman; Klaas Kok; Arja Ter Elst; Ed Schuuring; Léon C van Kempen; Wim Timens; T Jeroen N Hiltermann; Harry J M Groen; Anke van den Berg; Anthonie J van der Wekken
Journal:  Lung Cancer       Date:  2020-06-04       Impact factor: 5.705

10.  AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer.

Authors:  Darren A E Cross; Susan E Ashton; Serban Ghiorghiu; Cath Eberlein; Caroline A Nebhan; Paula J Spitzler; Jonathon P Orme; M Raymond V Finlay; Richard A Ward; Martine J Mellor; Gareth Hughes; Amar Rahi; Vivien N Jacobs; Monica Red Brewer; Eiki Ichihara; Jing Sun; Hailing Jin; Peter Ballard; Katherine Al-Kadhimi; Rachel Rowlinson; Teresa Klinowska; Graham H P Richmond; Mireille Cantarini; Dong-Wan Kim; Malcolm R Ranson; William Pao
Journal:  Cancer Discov       Date:  2014-06-03       Impact factor: 39.397

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  3 in total

Review 1.  Preclinical Models for Acquired Resistance to Third-Generation EGFR Inhibitors in NSCLC: Functional Studies and Drug Combinations Used to Overcome Resistance.

Authors:  Emna Mahfoudhi; Charles Ricordel; Gwendoline Lecuyer; Cécile Mouric; Hervé Lena; Rémy Pedeux
Journal:  Front Oncol       Date:  2022-04-07       Impact factor: 5.738

Review 2.  Acquired Mechanisms of Resistance to Osimertinib-The Next Challenge.

Authors:  Alejandro Ríos-Hoyo; Laura Moliner; Edurne Arriola
Journal:  Cancers (Basel)       Date:  2022-04-12       Impact factor: 6.575

Review 3.  Drug Tolerance to EGFR Tyrosine Kinase Inhibitors in Lung Cancers with EGFR Mutations.

Authors:  Kenichi Suda; Tetsuya Mitsudomi
Journal:  Cells       Date:  2021-06-24       Impact factor: 6.600

  3 in total

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