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The Lung Cancer Autochthonous Model Gene Expression Database Enables Cross-Study Comparisons of the Transcriptomic Landscapes Across Mouse Models

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

Research output: Contribution to journalArticlepeer-review

Abstract

Lung cancer, the leading cause of cancer mortality, exhibits diverse histologic 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. In this study, we established the Lung Cancer Autochthonous Model Gene Expression Database (LCAMGDB), an extensive repository of 1,354 samples from 77 transcriptomic datasets covering 974 samples from genetically engineered mouse models (GEMM), 368 samples from carcinogen-induced models, and 12 samples from a spontaneous model. Meticulous curation and collaboration with data depositors produced a robust and comprehensive database, enhancing the fidelity of the genetic landscape it depicts. The LCAMGDB aligned 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 the GEMMs. To accompany this resource, a web application was developed that offers researchers intuitive tools for in-depth gene expression analysis. With standardized reprocessing of gene expression data, the LCAMGDB 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.

Original languageEnglish (US)
Pages (from-to)1769-1783
Number of pages15
JournalCancer Research
Volume85
Issue number10
DOIs
StatePublished - May 15 2025

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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