作者
Yuan Liu,Manendra B. Lankadasari,Joel Rosiene,Kevin B. Johnson,Juan Zhou,Samhita Bapat,Lai-Fong L. Chow-Tsang,Huasong Tian,Brooke Mastrogiacomo,Di He,James G. Connolly,Harry B. Lengel,Raul Caso,Elizabeth G. Dunne,Cameron N. Fick,Gaetano Rocco,Smita Sihag,James M. Isbell,Matthew Bott,Bob T. Li,Piro Lito,Cameron Brennan,Mark H. Bilsky,Natasha Rekhtman,Prasad S. Adusumilli,Marty W. Mayo,Marcin Imielinski,David R. Jones
摘要
Approximately 50% of patients with surgically resected early-stage lung cancer develop distant metastasis. At present, there is no in vivo metastasis model to investigate the biology of human lung cancer metastases. Using well-characterized lung adenocarcinoma (LUAD) patient-derived organoids (PDOs), we establish an in vivo metastasis model that preserves the biologic features of human metastases. Results of whole-genome and RNA sequencing establish that our in vivo PDO metastasis model can be used to study clonality and tumor evolution and to identify biomarkers related to organotropism. Investigation of the response of KRAS