CRISPR Screening Identifies Mechanisms of Resistance to KRASG12C and SHP2 Inhibitor Combinations in Non-Small Cell Lung Cancer

被引：8

作者：

Prahallad, Anirudh ^{[1
]}

Weiss, Andreas ^{[1
]}

Voshol, Hans ^{[1
]}

Kerr, Grainne ^{[1
]}

Sprouffske, Kathleen ^{[1
]}

Yuan, Tina ^{[2
]}

Ruddy, David ^{[2
]}

Meistertzheim, Morgane ^{[1
]}

Kazic-Legueux, Malika ^{[1
]}

Kottarathil, Tina ^{[1
]}

Piquet, Michelle ^{[2
]}

Cao, Yichen ^{[2
]}

Martinuzzi-Duboc, Laetitia ^{[1
]}

Buhles, Alexandra ^{[1
]}

Adler, Flavia ^{[1
]}

Mannino, Salvatore ^{[1
]}

Tordella, Luca ^{[1
]}

Sansregret, Laurent ^{[1
]}

Maira, Sauveur-Michel ^{[1
]}

Graus Porta, Diana ^{[1
]}

Fedele, Carmine ^{[2
]}

Brachmann, Saskia M. ^{[1
,3
]}

机构：

[1] Novartis Inst Biomed Res, Basel, Switzerland

[2] Novartis Inst BioMed Res, Cambridge, MA USA

[3] NIBR, WSJ-386-3-13-01,Kohlenstr 84, CH-4056 Basel, Switzerland

来源：

CANCER RESEARCH | 2023年 / 83卷 / 24期

关键词：

RAS; P110-ALPHA; DRIVEN; POTENT;

D O I：

10.1158/0008-5472.CAN-23-1127

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Although KRAS(G12C) inhibitors show clinical activity in patients with KRAS G12C mutated non-small cell lung cancer (NSCLC) and other solid tumor malignancies, response is limited by multiple mechanisms of resistance. The KRAS(G12C) inhibitor JDQ443 shows enhanced preclinical antitumor activity combined with the SHP2 inhibitor TNO155, and the combination is currently under clinical evaluation. To identify rational combination strategies that could help overcome or prevent some types of resistance, we evaluated the duration of tumor responses to JDQ443 +/- TNO155, alone or combined with the PI3K alpha inhibitor alpelisib and/or the cyclin-dependent kinase 4/6 inhibitor ribociclib, in xenograft models derived from a KRAS(G12C)-mutant NSCLC line and investigated the genetic mechanisms associated with loss of response to combined KRAS(G12C)/SHP2 inhibition. Tumor regression by single-agent JDQ443 at clinically relevant doses lasted on average 2 weeks and was increasingly extended by the double, triple, or quadruple combinations. Growth resumption was accompanied by progressively increased KRAS G12C amplification. Functional genome-wide CRISPR screening in KRAS(G12C)-dependent NSCLC lines with distinct mutational profiles to identify adaptive mechanisms of resistance revealed sensitizing and rescuing genetic interactions with KRAS(G12C)/SHP2 coinhibition; FGFR1 loss was the strongest sensitizer, and PTEN loss the strongest rescuer. Consistently, the antiproliferative activity of KRAS(G12C)/SHP2 inhibition was strongly enhanced by PI3K inhibitors. Overall, KRAS G12C amplification and alterations of the MAPK/PI3K pathway were predominant mechanisms of resistance to combined KRAS(G12C)/SHP2 inhibitors in preclinical settings. The biological nodes identified by CRISPR screening might provide additional starting points for effective combination treatments. Significance: Identification of resistance mechanisms to KRAS(G12C)/SHP2 coinhibition highlights the need for additional combination therapies for lung cancer beyond on-pathway combinations and offers the basis for development of more effective combination approaches.

引用

页码：4130 / 4141

页数：12

共 21 条

[21] Brigatinib in Japanese patients with tyrosine kinase inhibitor-naive ALK-positive non-small cell lung cancer: first results from the phase 2 J-ALTA study
Sugawara, Shunichi
Kondo, Masashi
Yokoyama, Toshihide
Kumagai, Toru
Nishio, Makoto
Goto, Koichi
Nakagawa, Kazuhiko
Seto, Takashi
Yamamoto, Nobuyuki
Kudou, Kentarou
Asato, Takayuki
Zhang, Pingkuan
Ohe, Yuichiro
INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY, 2022, 27 (12) : 1828 - 1838

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