A Lung Cancer Mouse Model Database

Ling Cai, Ying Gao,Ralph J DeBerardinis大牛学者,George Acquaah-Mensah,Vassilis Aidinis,Jennifer E Beane,Shyam Biswal大牛学者,Ting Chen, Carla P Concepcion-Crisol,Barbara M Grüner,Deshui Jia, Robert Jones,Jonathan M Kurie大牛学者, Min Gyu Lee, Per Lindahl, Yonathan Lissanu, Maria Corina Lorz Lopez,Rosanna Martinelli,Pawel K Mazur,Sarah A Mazzilli,Shinji Mii,Herwig Moll,Roger Moorehead,Edward E Morrisey大牛学者,Sheng Rong Ng,Matthew G Oser, Arun R Pandiri, Charles A Powell, Giorgio Ramadori,Mirentxu Santos Lafuente,Eric Snyder,Rocio Sotillo, Kang-Yi Su,Tetsuro Taki, Kekoa Taparra, Yifeng Xia, Ed van Veen,Monte M Winslow,Guanghua Xiao大牛学者,Charles M Rudin大牛学者,Trudy G Oliver,Yang Xie大牛学者,John D Minna大牛学者

bioRxiv the preprint server for biology(2024)

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摘要
Lung cancer, the leading cause of cancer mortality, exhibits diverse histological subtypes and genetic complexities. Numerous preclinical mouse models have been developed to study lung cancer, but data from these models are disparate, siloed, and difficult to compare in a centralized fashion. Here we established the Lung Cancer Mouse Model Database (LCMMDB), an extensive repository of 1,354 samples from 77 transcriptomic datasets covering 974 samples from genetically engineered mouse models (GEMMs), 368 samples from carcinogen-induced models, and 12 samples from a spontaneous model. Meticulous curation and collaboration with data depositors have produced a robust and comprehensive database, enhancing the fidelity of the genetic landscape it depicts. The LCMMDB aligns 859 tumors from GEMMs with human lung cancer mutations, enabling comparative analysis and revealing a pressing need to broaden the diversity of genetic aberrations modeled in GEMMs. Accompanying this resource, we developed a web application that offers researchers intuitive tools for in-depth gene expression analysis. With standardized reprocessing of gene expression data, the LCMMDB serves as a powerful platform for cross-study comparison and lays the groundwork for future research, aiming to bridge the gap between mouse models and human lung cancer for improved translational relevance.
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