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XPO1-dependent nuclear export is a druggable vulnerability in KRAS-mutant lung cancer
Open accessAbstract
The common participation of oncogenic KRAS proteins in many of the most lethal human cancers, together with the ease of detecting somatic KRAS mutant alleles in patient samples, has spurred persistent and intensive efforts to develop drugs that inhibit KRAS activity. However, advances have been hindered by the pervasive inter- and intra-lineage diversity in the targetable mechanisms that underlie KRAS-driven cancers, limited pharmacological accessibility of many candidate synthetic-lethal interactions and the swift emergence of unanticipated resistance mechanisms to otherwise effective targeted therapies. Here we demonstrate the acute and specific cell-autonomous addiction of KRAS-mutant non-small-cell lung cancer cells to receptor-dependent nuclear export. A multi-genomic, data-driven approach, utilizing 106 human non-small-cell lung cancer cell lines, was used to interrogate 4,725 biological processes with 39,760 short interfering RNA pools for those selectively required for the survival of KRAS-mutant cells that harbour a broad spectrum of phenotypic variation. Nuclear transport machinery was the sole process-level discriminator of statistical significance. Chemical perturbation of the nuclear export receptor XPO1 (also known as CRM1), with a clinically available drug, revealed a robust synthetic-lethal interaction with native or engineered oncogenic KRAS both in vitro and in vivo. The primary mechanism underpinning XPO1 inhibitor sensitivity was intolerance to the accumulation of nuclear IκBα (also known as NFKBIA), with consequent inhibition of NFκB transcription factor activity. Intrinsic resistance associated with concurrent FSTL5 mutations was detected and determined to be a consequence of YAP1 activation via a previously unappreciated FSTL5-Hippo pathway regulatory axis. This occurs in approximately 17% of KRAS-mutant lung cancers, and can be overcome with the co-administration of a YAP1-TEAD inhibitor. These findings indicate that clinically available XPO1 inhibitors are a promising therapeutic strategy for a considerable cohort of patients with lung cancer when coupled to genomics-guided patient selection and observation.
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“The pervasive diversity of this oncogenotype was aptly demonstrated in a study that applied affinity propagation clustering analysis36 to mRNA expression data from 106 genomically-annotated NSCLC cell lines; strikingly, variation in mRNA expression within KRAS-mutant NSCLC cell lines was equivalent to that observed across the entire cell line panel37.”
From Co-occurring genomic alterations in non-small-cell lung cancer biology and therapy (2019) · cites this paper as [37]
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High XPO1 Expression can Stratify Gastric Cancer Patients with Poor Clinical Outcome
(2024) · Cancer Studies and Therapeutics · doi:10.31038/cst.2024921
Exporting nuclear export inhibitors from hematologic to solid tumour malignancies
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Therapeutic Targeting of KRAS Oncogene in Pancreatic Ductal Adenocarcinoma (PDAC)
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Metadata
- Authors
- Kim, J., McMillan, E., Kim, H. S., Venkateswaran, N., Makkar, G., Rodriguez-Canales, J., Villalobos, P., Neggers, J. E., Mendiratta, S., Wei, S., Landesman, Y., Senapedis, W., Baloglu, E., Chow, C.-W. B., Frink, R. E., Gao, B., Roth, M., Minna, J. D., Daelemans, D., Wistuba, I. I., Posner, B. A., Scaglioni, P. P., & White, M. A.
- Affiliations
- Yonsei University (KR)
- The University of Texas MD Anderson Cancer Center (US)
- KU Leuven (BE)
- Karyopharm Therapeutics (United States) (US)
- Corresponding author
- White, Michael A.
- ORCID
- Venue
- Nature
- Published
- 2016-09-28
- Volume
- 538
- Issue
- 7623
- Pages
- 114-117
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5161658
- OpenAlex
- W2526506448
- Cited by
- 202
- References
- 36
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 22 · 2023: 13 · 2022: 23 · 2021: 18 · 2020: 27 · 2019: 23 · 2018: 32 · 2017: 25 · 2016: 1
- FWCI
- 14.04
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- YUHSpace (Yonsei University Medical Library) (submittedVersion, cc-by-nc-nd)
- RePEc: Research Papers in Economics (submittedVersion)
- Lirias (KU Leuven) (submittedVersion)
- Funders
- Cancer Prevention and Research Institute of Texas
- National Cancer Institute (P50CA070907, U01CA176284, RC2CA148225)
- National Institute of General Medical Sciences (T32GM008203)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- CRM1, nuclear export, KRAS-mutant lung cancer, non-small cell lung cancer, synthetic lethality, NF-κB, IκBα, YAP, Hippo signaling pathway, verteporfin, drug resistance, RNAi screen, cell lines, KRAS inhibitors
- MeSH terms
- NF-KappaB Inhibitor alpha, Verteporfin, Hippo Signaling Pathway, YAP-Signaling Proteins, TEA Domain Transcription Factors, Exportin 1 Protein, Animals, Carcinoma, Non-Small-Cell Lung, Cell Nucleus, Cell Survival, DNA-Binding Proteins, Female, Genes, Lethal, Humans, Lung Neoplasms, Mutation, Nuclear Proteins, Phosphoproteins, Porphyrins, Transcription Factors, Signal Transduction, Proto-Oncogene Proteins p21(ras), NF-kappa B, Protein Serine-Threonine Kinases, Receptors, Cytoplasmic and Nuclear, Active Transport, Cell Nucleus, Xenograft Model Antitumor Assays, Karyopherins, RNA Interference, RNA, Small Interfering, Follistatin-Related Proteins, Cell Line, Tumor, Adaptor Proteins, Signal Transducing, Cell Proliferation, Mice
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