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Loss of p53 and mutational heterogeneity drives immune resistance in an autochthonous mouse lung cancer model with high tumor mutational burden
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“In other words, functional wild-type p53 promotes a cancer-suppressing TME in tumor cells, whereas a decrease in or loss of wild-type p53 promotes a cancer-promoting TME in tumor cells.”
From p53: from understanding its structure to advances in therapeutic targeting (2026) · cites this paper as [129]
In the citing paper
“Recently, several studies have shown a correlation between p53 expression and the efficacy of tumor immunotherapy, which also indicates that the status of p53 affects the TME128–130 (Fig. 3).”
From p53: from understanding its structure to advances in therapeutic targeting (2026) · cites this paper as [129]
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“In some cases, mutant p53 can also modulate the tumor microenvironment by interacting with immune cells, further enhancing tumor invasiveness.129”
From p53: from understanding its structure to advances in therapeutic targeting (2026) · cites this paper as [129]
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Cites
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Li, H. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty191 · Cited by 14,807
Pembrolizumab plus chemotherapy in metastatic non–small-cell lung cancer
Gandhi, L., Rodríguez-Abreu, D., Gadgeel, S., Esteban, E., Felip, E., De Angelis, F., Domine, M., Clingan, P., Hochmair, M. J., Powell, S. F., et al. (2018) · New England Journal of Medicine · doi:10.1056/nejmoa1801005 · Cited by 6,607
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Tumor mutational load predicts survival after immunotherapy across multiple cancer types
Samstein, R. M., Lee, C.-H., Shoushtari, A. N., Hellmann, M. D., Shen, R., Janjigian, Y. Y., Barron, D. A., Zehir, A., Jordan, E. J., Omuro, A., et al. (2019) · Nature Genetics · doi:10.1038/s41588-018-0312-8 · Cited by 4,071
Next-generation characterization of the Cancer Cell Line Encyclopedia
Ghandi, M., Huang, F. W., Jané-Valbuena, J., Kryukov, G. V., Lo, C. C., McDonald, E. R., Barretina, J., Gelfand, E. T., Bielski, C. M., Li, H., et al. (2019) · Nature · doi:10.1038/s41586-019-1186-3 · Cited by 3,394
Self-citationSTK11/LKB1 Mutations and PD-1 Inhibitor Resistance in KRAS -Mutant Lung Adenocarcinoma
Skoulidis, F., Goldberg, M. E., Greenawalt, D. M., Hellmann, M. D., Awad, M. M., Gainor, J. F., Schrock, A. B., Hartmaier, R. J., Trabucco, S. E., Gay, L., et al. (2018) · Cancer Discovery · doi:10.1158/2159-8290.cd-18-0099 · Cited by 1,641
Self-citationMutational signatures associated with tobacco smoking in human cancer
Alexandrov, L. B., Ju, Y. S., Haase, K., Van Loo, P., Martincorena, I., Nik-Zainal, S., Totoki, Y., Fujimoto, A., Nakagawa, H., Shibata, T., et al. (2016) · Science · doi:10.1126/science.aag0299 · Cited by 1,100
p53 in the DNA–Damage–Repair Process
Williams, A. B., & Schumacher, B. (2016) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a026070 · Cited by 835
The distribution of cellular turnover in the human body
Sender, R., & Milo, R. (2021) · Nature Medicine · doi:10.1038/s41591-020-01182-9 · Cited by 420
DNA Sensing in Mismatch Repair-Deficient Tumor Cells Is Essential for Anti-tumor Immunity
Lu, C., Guan, J., Lu, S., Jin, Q., Rousseau, B., Lu, T., Stephens, D., Zhang, H., Zhu, J., Yang, M., et al. (2021) · Cancer Cell · doi:10.1016/j.ccell.2020.11.006 · Cited by 285
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p53: from understanding its structure to advances in therapeutic targeting
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Dynamic STING repression orchestrates immune cell development and function
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Metadata
- Authors
- Zhu, M., Kim, J., Deng, Q., Ricciuti, B., Alessi, J. V., Eglenen-Polat, B., Bender, M. E., Huang, H.-C., Kowash, R. R., Cuevas, I., Bennett, Z. T., Gao, J., Minna, J. D., Castrillon, D. H., Awad, M. M., Xu, L., & Akbay, E. A.
- Venue
- Cancer Cell
- Publisher
- Elsevier BV
- Published
- 2023-10
- Volume
- 41
- Issue
- 10
- Pages
- 1731-1748.e8
- ISSN
- 1535-6108
- Cited by
- 71
- References
- 12
- Language
- en
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 374 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Funders
- Welch Foundation (1975-20190330)
- Mary Kay Ash Foundation
- National Institutes of Health (R01CA237405, R01CA265884, RP180770, RP210099)
- AstraZeneca
- U.S. Department of Defense (W81XWH-21-1-0856)
- Cancer Prevention and Research Institute of Texas (RR160080)
- American Cancer Society (RSG-22-051-01-IBCD)
- A Breath of Hope Lung Foundation
- National Cancer Institute (5P50CA070907, R01CA276058)
- National Comprehensive Cancer Network Foundation (NCCN 2021)
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- The paper
- Zhu, M., Kim, J., Deng, Q., Ricciuti, B., Alessi, J. V., Eglenen-Polat, B., Bender, M. E., Huang, H.-C., Kowash, R. R., Cuevas, I., Bennett, Z. T., Gao, J., Minna, J. D., Castrillon, D. H., Awad, M. M., Xu, L., & Akbay, E. A. (2023). Loss of p53 and mutational heterogeneity drives immune resistance in an autochthonous mouse lung cancer model with high tumor mutational burden. Cancer Cell. https://doi.org/10.1016/j.ccell.2023.09.006
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