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hnRNP K Is a Haploinsufficient Tumor Suppressor that Regulates Proliferation and Differentiation Programs in Hematologic Malignancies
Open accessAbstract
hnRNP K regulates cellular programs, and changes in its expression and mutational status have been implicated in neoplastic malignancies. To directly examine its role in tumorigenesis, we generated a mouse model harboring an Hnrnpk knockout allele (Hnrnpk(+/-)). Hnrnpk haploinsufficiency resulted in reduced survival, increased tumor formation, genomic instability, and the development of transplantable hematopoietic neoplasms with myeloproliferation. Reduced hnRNP K expression attenuated p21 activation, downregulated C/EBP levels, and activated STAT3 signaling. Additionally, analysis of samples from primary acute myeloid leukemia patients harboring a partial deletion of chromosome 9 revealed a significant decrease in HNRNPK expression. Together, these data implicate hnRNP K in the development of hematological disorders and suggest hnRNP K acts as a tumor suppressor.
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“In addition, the expression of hnRNP K (40), SRSF3 (SRp20) (41), and YB-1 (42) has been shown to be altered in AML, but also to contribute to leukemia progression.”
From Discovery of a Novel CIP2A Variant (NOCIVA) with Clinical Relevance in Predicting TKI Resistance in Myeloid Leukemias (2021) · cites this paper as [40]
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hnRNPK-derived cell-penetrating peptide inhibits cancer cell survival
Pavan Kumar, P., Buczkowski, S. A., & Moon, A. (2021) · Molecular Therapy — Oncolytics · doi:10.1016/j.omto.2021.10.004 · Cited by 8
Assessing the role of intrinsic disorder in RNA-binding protein function: hnRNP K as a case study
Malaney, P., Benitez, O., Zhang, X., & Post, S. M. (2022) · Methods · doi:10.1016/j.ymeth.2022.10.009 · Cited by 8
Self-citationRemoval of Nonspecific Binding Proteins is Required in Co-Immunoprecipitation with Nuclear Proteins
Zeng, X., Zeng, W.-H., Zhou, J., Liu, X., Huang, G. C., Zhu, H. M., Xiao, S., Zeng, Y., & Cao, D. (2022) · BioTechniques · doi:10.2144/btn-2022-0048 · Cited by 8
Hoff, F. W., Hu, C. W., Qutub, A. A., Qiu, Y., Aitken, M. J. L., Bueso-Ramos, C., Abbas, H. A., Post, S. M., de Bont, E. S. J. M., & Kornblau, S. M. (2019) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.201800133 · Cited by 8
Self-citationInsights into the role of hnRNPK in spermatogenesis via the piRNA pathway
Xu, H., Guo, J., Huang, Y., Zhang, M., Wang, Y., Li, X., Cheng, X., Meng, T., Hao, R., Wei, X., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-91081-1 · Cited by 7
Sun, D., Zhao, X., Yu, Y., Li, W., Gu, P., Zhi, Z., & Xu, D. (2022) · Bioscience Reports · doi:10.1042/bsr20212090 · Cited by 7
The RNA binding protein hnRNPK protects against adriamycin-induced podocyte injury
Zhao, S., Feng, J., Li, J., Cao, R., Zhang, Y., Yang, S., & Yin, L. (2021) · Annals of Translational Medicine · doi:10.21037/atm-21-3577 · Cited by 6
The tumor suppressor HNRNPK induces p53-dependent nucleolar stress to drive ribosomopathies
Aguilar-Garrido, P., Velasco‐Estevez, M., Navarro-Aguadero, M. Á., Otero, Á., Ibáñez-Navarro, M., Marugal, M. Á., Hernández‐Sánchez, M., Malaney, P., Rodriguez, A., Benitez, O., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci183697 · Cited by 7
Self-citationRecruitment of chromatin remodelers by XIST B-repeat region is variably dependent on HNRNPK
Navarro-Cobos, M. J., & Brown, C. J. (2024) · Human Molecular Genetics · doi:10.1093/hmg/ddae173 · Cited by 6
Postlmayr, A., & Wutz, A. (2017) · Journal of Molecular Biology · doi:10.1016/j.jmb.2017.03.013 · Cited by 6
Jin, L., Li, T., Hong, Y., Mao, R., Li, X., Zhu, C., Mu, J., Zhou, J., Pan, L., Que, Y., et al. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115703 · Cited by 6
Metadata
- Authors
- Gallardo, M., Lee, H. J., Zhang, X., Bueso-Ramos, C., Pageon, L. R., McArthur, M., Multani, A., Nazha, A., Manshouri, T., Parker-Thornburg, J., Rapado, I., Quintas-Cardama, A., Kornblau, S. M., Martinez-Lopez, J., & Post, S. M.
- Affiliations
- The University of Texas MD Anderson Cancer Center (US)
- Hospital Universitario 12 De Octubre (ES)
- Corresponding author
- Post, Sean M.
- ORCID
- Venue
- Cancer Cell
- Publisher
- Elsevier BV
- Published
- 2015-10
- Volume
- 28
- Issue
- 4
- Pages
- 486-499
- ISSN
- 1535-6108 (ISSN-L)
- PMC
- PMC4652598
- OpenAlex
- W2168139795
- Cited by
- 145
- References
- 36
- Citations by year
- 2026: 11 · 2025: 12 · 2024: 4 · 2023: 15 · 2022: 15 · 2021: 21 · 2020: 13 · 2019: 22 · 2018: 14 · 2017: 12 · 2016: 5 · 2015: 1
- FWCI
- 8.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cancer Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- University of Texas MD Anderson Cancer Center
- National Cancer Institute (P50CA100632, CA-16672, P50 CA1000632-09, P30CA016672)
- Topics
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Keywords
- hnRNP K, haploinsufficiency, tumor suppressor, hematologic malignancies, acute myeloid leukemia, chromosome 9 deletion, myeloproliferation, STAT3 signaling, p21, C/EBP, genomic instability, cell proliferation, cell differentiation
- MeSH terms
- Animals, Cell Differentiation, Cells, Cultured, Chromosomes, Human, Pair 9, Humans, Ribonucleoproteins, Signal Transduction, Gene Expression Regulation, Neoplastic, Survival Analysis, Hematologic Neoplasms, Heterogeneous-Nuclear Ribonucleoprotein K, Chromosomal Instability, Cell Proliferation, Mice, Gene Knockout Techniques, Haploinsufficiency
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