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Nature · 2026

A dependency map enhanced with next-generation 3D cancer models.

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Neiswender James V, Maffa Samuel, Brenan Lisa, ElHarouni Dina, Yun Yejie, Boyle Isabella, Wienand Kirsty, Inam Haider, Bertea Tate, Anderson Ashley, Wong Megan, Enriquez Matias, Lenz Evan, Villafranca Beatriz, Shanks Nora, Hager Mary, Lloyd Nia, Shadmany Hannah, Wie Sarah J, Liang Harry, Yunghans Konnor, Zhang Xiaomeng, Golden Lauren, Harris Hannah, Day Serena, Montgomery Philip, Stokes Samantha, Giglio Ross M, Hajal Cynthia, Whittle James R, Garcia Guadalupe, Mills Caitlin E, Touat Mehdi, Pelton Kristine, Li Hongyu, Prabhakar Prem Sai, Herter Sonja, Kamrat Zoe Hoffmann, Gui Dan, Dilly Julien, Wong Chen Khuan, Guo Jimmy A, Pal Sangita, Baidi Yossef, Johnston Ryan, Brown Daniel D, Bhatia Sonam, Winter Peter S, Raghavan Srivatsan, Beroukhim Rameen, Colas Eva, Spector David L, Bass Adam J, Sorger Peter K, Chen Yu, Hill Sarah J, Oesterreich Steffi, Lee Adrian V, Beltran Himisha, Boehm Jesse S, Tseng Yuen-Yi, Root David E, Hahn William C, Aguirre Andrew J, Campbell Catarina D, Ligon Keith L, Dempster Joshua M, Shibue Tsukasa, Vazquez Francisca

Аннотация

Despite advances in precision oncology, effective personalized treatments are still lacking for most patients with cancer1. The Cancer Dependency Map (DepMap) accelerates this field by systematically identifying cancer vulnerabilities in diverse preclinical models. Data from over 1,300 cell lines have led to the discovery of new therapeutic strategies across multiple tumour types2. However, mapping cancer vulnerabilities using traditional cell lines has limitations, including insufficient cancer subtype representation and the impact of culture conditions on perturbation responses. Here we perform 147 genome-scale CRISPR screens and multi-omic characterizations of next-generation (NextGen) cancer models (organoids and spheroids) across 10 cancer types. This strategy enables the expansion of DepMap to cover new genomic and molecular subtypes and to identify new biomarker-associated vulnerabilities. These new models also preserve transcriptional programs that are silenced in traditional cell lines and facilitate the discovery of specific gene dependencies associated with these programs. Comparisons of traditional and NextGen cancer models enable further identification of distinct effects of growth format and culture medium on gene essentiality. The integrated dataset combines data from both model types to offer a valuable, expansive resource for exploring cancer vulnerabilities and is accessible via the DepMap portal.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты