The DOI matches its Crossref record; 59 of the 60 references it cites were found in a registry or an index.
p53 engages the cGAS/STING cytosolic DNA sensing pathway for tumor suppression
Open accessPublished version of a preprint
Abstract
Tumor suppression by TP53 involves cell-autonomous and non-cell-autonomous mechanisms. TP53 can suppress tumor growth by modulating immune system functions; however, the mechanistic basis for this activity is not well understood. We report that p53 promotes the degradation of the DNA exonuclease TREX1, resulting in cytosolic dsDNA accumulation. We demonstrate that p53 requires the ubiquitin ligase TRIM24 to induce TREX1 degradation. The cytosolic DNA accumulation resulting from TREX1 degradation activates the cytosolic DNA-sensing cGAS/STING pathway, resulting in induction of type I interferons. TREX1 overexpression sufficed to block p53 activation of the cGAS/STING pathway. p53-mediated induction of type I interferon (IFNB1) is suppressed by cGAS/STING knockout, and p53's tumor suppressor activities are compromised by the loss of signaling through the cGAS/STING pathway. Thus, our study reveals that p53 utilizes the cGAS/STING innate immune system pathway for both cell-intrinsic and cell-extrinsic tumor suppressor activities.
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“Links between IL-1 signalling and p53 have been reported in the context of tumour cells 68,69 , and the cGAS-STING axis is increasingly linked to DNA damage 70 , although the exact triggers of this pathway in the context of AAV-mediated CNS transduction remain to be defined.”
From AAV vectors trigger DNA damage response-dependent pro-inflammatory signalling in human iPSC-derived CNS models and mouse brain (2025) · cites this paper as [70]
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Citations
Cites
Hallmarks of Cancer: The Next Generation
Hanahan, D., & Weinberg, R. A. (2011) · Cell · doi:10.1016/j.cell.2011.02.013 · Cited by 66,590
Genome-scale CRISPR-Cas9 knockout screening in human cells
Shalem, O., Sanjana, N. E., Hartenian, E., Shi, X., Scott, D. A., Mikkelsen, T. S., Heckl, D., Ebert, B. L., Root, D. E., Doench, J. G., et al. (2014) · Science · doi:10.1126/science.1247005 · Cited by 5,234
Cyclic GMP-AMP Synthase Is a Cytosolic DNA Sensor That Activates the Type I Interferon Pathway
Sun, L., Wu, J., Du, F., Chen, X., & Chen, Z. J. (2013) · Science · doi:10.1126/science.1232458 · Cited by 4,996
Seth, R. B., Sun, L., Ea, C.-K., & Chen, Z. J. (2005) · Cell · doi:10.1016/j.cell.2005.08.012 · Cited by 3,329
IKKε and TBK1 are essential components of the IRF3 signaling pathway
Fitzgerald, K. A., McWhirter, S. M., Faia, K. L., Rowe, D. C., Latz, E., Golenbock, D. T., Coyle, A. J., Liao, S.-M., & Maniatis, T. (2003) · Nature Immunology · doi:10.1038/ni921 · Cited by 2,680
Cyclic GMP-AMP Is an Endogenous Second Messenger in Innate Immune Signaling by Cytosolic DNA
Wu, J., Sun, L., Chen, X., Du, F., Shi, H., Chen, C., & Chen, Z. J. (2012) · Science · doi:10.1126/science.1229963 · Cited by 2,628
IPS-1, an adaptor triggering RIG-I- and Mda5-mediated type I interferon induction
Kawai, T., Takahashi, K., Sato, S., Coban, C., Kumar, H., Kato, H., Ishii, K. J., Takeuchi, O., & Akira, S. (2005) · Nature Immunology · doi:10.1038/ni1243 · Cited by 2,562
Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas
Xue, W., Zender, L., Miething, C., Dickins, R. A., Hernando, E., Krizhanovsky, V., Cordon-Cardo, C., & Lowe, S. W. (2007) · Nature · doi:10.1038/nature05529 · Cited by 2,473
T antigen is bound to a host protein in SY40-transformed cells
Lane, D. P., & Crawford, L. V. (1979) · Nature · doi:10.1038/278261a0 · Cited by 2,456
Cardif is an adaptor protein in the RIG-I antiviral pathway and is targeted by hepatitis C virus
Meylan, E., Curran, J., Hofmann, K., Moradpour, D., Binder, M., Bartenschlager, R., & Tschopp, J. (2005) · Nature · doi:10.1038/nature04193 · Cited by 2,401
Cited by
Sorted by citations
Items 101–167 of 167
Wang, X., Liu, L., Tian, J., Kong, Z., Lv, F., Yan, J., Li, S., Ma, Z., Guo, D., Wang, Y., et al. (2026) · ACS Nano · doi:10.1021/acsnano.5c21154 · Cited by 3
Recent progress in cGAS–STING agonist design and mechanisms of cancer immune modulation
Wang, L., Nafees, M., Fei, H., Hanif, M., & Yang, P. (2026) · RSC Chemical Biology · doi:10.1039/d6cb00005c · Cited by 3
Molecular mechanisms regulating cGAS/STING activation in health and disease
Cho, M.-G., Lee, R., Johnson, J., & Gupta, G. P. (2026) · Journal of Clinical Investigation · doi:10.1172/jci204548 · Cited by 4
“Radio-therapy is commonly employed to induce DNA damage for tumor control, which has been shown to induce cGAS-mediated innate p53 has been shown to mediate degradation of TREX1 to activate cGAS and prevent oncogenic transformation (59).”
Targeting transcription-replication conflicts using G-quadruplexes stabilizers in multiple myeloma
Dutrieux, L., Ovejero, S., Guillemin, A., Zellagui, M. L., Bruyne, E. D., Muylaert, C., Hemelrijck, L. A. V., Lin, Y., Loughran, E., Choquet, A., et al. (2025) · Blood Neoplasia · doi:10.1016/j.bneo.2025.100072 · Cited by 3
Stange, C., Dreyer, T. F., Riedel, M., Elsen, F. A. V., Seitz, S., Hamann, D., Kiechle, M. B., & Bronger, H. (2025) · British Journal of Cancer · doi:10.1038/s41416-025-03076-4 · Cited by 3
“Activity assay results represent the mean, error bars are SEM, signi fi cant differences were determined by Welch ’ s ANOVA with Tamhane ’ s T2 multiple comparisons test. observations are consistent with publicly available data from the KM plotter when patients are strati fi ed according to their…”
Bioinformatic Analysis of Roquin Family Reveals Their Potential Role in Immune System
Li, X., Yang, S., Zhang, X., Zhang, Y., Zhang, Y., & Li, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25115859 · Cited by 3
“As a result, abnormal gene expression leads to developmental defects and imbalanced immune responses [1–3].”
BackgroundTargeting P53 Gene in Breast Cancer
Abuhagr, A. M., Musa, E. B., Attir, O. A., & Alati, R. M. O. (2023) · Journal Of Advanced Zoology · doi:10.17762/jaz.v44is7.2746 · Cited by 2
Dong, Y.-D., Wu, X., Liu, W., Hu, Y., Zhang, H., Fang, W., & Luo, Q. (2025) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v17.i6.105782 · Cited by 2
“With the deepening of research on TP53 , more and more studies have shown that TP53 was also closely related to tumor metabolism[27,28], ferroptosis[29,30], stem cell dynamic[31,32], cell competition[33,34], epithelial-mesenchymal transition [35,36] and immunity[37,38].”
Isoliensinine inhibits mitophagy and sensitizes T cell malignancies for STING-mediated NK clearance
Ge, X., Yang, G., Zhu, Y., Chen, H., Zheng, G., Cao, J., Qing, Y., Shen, S., Pan, Y., & Hu, P. (2025) · Acta Pharmacologica Sinica · doi:10.1038/s41401-025-01636-1 · Cited by 2
“It has thus been proposed that enhancing cytosolic dsDNA production by damaging DNA may promote immune response [10].”
Zhang, Y., Han, Y., Li, S., Shan, R., Lin, L., Gu, Z., wang, R., Chen, Y., Xiao, J., an, F., et al. (2026) · Redox Biology · doi:10.1016/j.redox.2025.103993 · Cited by 2
“These transcriptional changes suggest that prenylterphenyllin promotes apoptosis in CRC cells by modulating key apoptosis-related pathways, with p53 playing a vital role in mediating this effect [51,52].”
Li, J., Jiang, W., Tu, G., Zhong, Z., Luo, Z., Horng, T., & Miao, C. (2026) · British Journal of Cancer · doi:10.1038/s41416-025-03319-4 · Cited by 2
Self-citationLuo, H., Wang, G., Liu, T., Guo, J., Li, Q., Cao, Z., Wang, R., & He, W. (2026) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2026.121319 · Cited by 2
A variant in long noncoding RNA NORSF affects granulosa cells response to transcription factor RFX7
Wang, M., Zhang, J., Sheng, W., Wu, W., Du, X., & Li, Q. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31414 · Cited by 2
“A recent study reported that wild ‐ type P53 can activate this innate immune signaling pathway by inducing the decay of DNA exonuclease TREX1 and cytosolic double ‐ stranded DNA accumulation (Ghosh et al., 2023).”
Tever, O. K., Mentrup, T., Chinn, I. K., Ishikuma, H., Fluhrer, R., Schmitz, M., Wehner, R., Behrendt, R., Chinen, J., & Schröder, B. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05645-5 · Cited by 2
Tumor suppressor genotype influences the extent and mode of immunosurveillance in lung cancer
Adler, K. M., Xu, H., Gladstein, A. C., Irizarry-Negron, V. M., Robertson, M. R., Doerig, K. R., Petrov, D. A., Winslow, M. M., & Feldser, D. M. (2026) · Nature Communications · doi:10.1038/s41467-026-74023-x · Cited by 1
Gigaxonin Potentiates Antiviral Innate Immune Responses by Targeting cGAS and TREX1
Ji, B., Wang, J., Tu, Y., Zhang, S., Wei, Y., He, Y., Zhang, B., Zhao, Q., Hu, H., & Liu, Y. (2025) · Advanced Science · doi:10.1002/advs.202507146 · Cited by 1
Singh, N. C., Yadav, N., Sharma, R. K., Gupta, P., Sarkar, J., & Mitra, K. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.10.264 · Cited by 1
Wu, T., Yu, Q. C., Wang, Y., Tang, H., & Guo, W. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115790 · Cited by 1
Wang, X., Zheng, X., Fang, Y., Zheng, T., Zhang, J., Li, Z., & Hou, Y. (2025) · CytoJournal · doi:10.25259/cytojournal_106_2025 · Cited by 1
“[23] Increasing evidence suggests that tumor cells evade host immune surveillance and establish an immunosuppressive microenvironment by inhibiting the activation of the cGAS-STING pathway.”
Wang, L., Dong, X., Yu, L., Jie, H., Wang, B., Li, L., Chen, J., Liu, M., & Dong, B. (2025) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2025185 · Cited by 1
“Among these proteins, the tripartite motif - containing (TRIM) protein family has drawn increasing attention, with TRIM24 in particular being reported to facilitate p53 ubiquitina - tion in cancer cells [24,25].”
Gu, Y., Wang, S., Xiao, Y., Li, Y., Weng, L., & Chen, K. (2026) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2026.105124 · Cited by 1
Targeting the cGAS-STING-TBK1 pathway in cancer therapy
Jiang, L., Zhong, Y., Zhang, Z., Yang, Q., Sun, S., Sun, H., & Liu, Z. (2026) · Future Medicinal Chemistry · doi:10.1080/17568919.2026.2628553 · Cited by 2
TBC1 domain family member 23 is essential for STING-mediated anti-melanoma effect
Niu, S., Li, G., Wei, P., Hu, X., Qin, J., Yuan, Y., Wang, J., Tu, Y., Zhao, L., Yu, L., et al. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00418-3 · Cited by 1
“The phosphorylated IRF3 forms dimers that translocate to the nucleus, where they induce transcription of IFN-I and interferon-stimulated genes (ISGs) [5, 21].”
Targeting the cGAS-STING pathway in ophthalmology: from innate immunity to therapeutic innovation
Yan, D., Ouyang, W., Li, K., & Sun, X. (2026) · Experimental Eye Research · doi:10.1016/j.exer.2026.110978 · Cited by 1
Borukaeva, I. K., Хараева, З. Ф., Tkhabisimova, I. K., Барасбиевич, Х. А., Алимбекович, У. Т., Shogenov, B. M., & Kunizhev, A. M. (2026) · Бюллетень Восточно-Сибирского научного центра Сибирского отделения Российской академии медицинских наук · doi:10.29413/abs.2026-11.1.11 · Cited by 1
Zheng, B., Yao, G., Pang, Y., Luo, J., Yang, Z., Xiu, F., Zhen, C., & Liang, R. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1850149 · Cited by 2
MDM2 binds and suppresses RNA polymerase III to restrain the innate immune response to cytosolic DNA
Weber, S., Manzini, V., Dietrich, H., Schotte, H., Moshkovskii, S. A., Hackert, P., Duman, E. T., Vu, N. Q., Prokakis, E., Salinas, G., et al. (2026) · Cell Death and Differentiation · doi:10.1038/s41418-026-01834-2 · Cited by 1
Qu, N., Guo, J., Zhang, M., Liu, M., Yu, C., Li, Y., 郑晨果, Li, X., Shi, Z., & Xie, J. (2026) · Journal of Controlled Release · doi:10.1016/j.jconrel.2026.115245 · Cited by 1
Lin, T., Chen, Y., & Huang, Z. (2026) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-026-05815-7 · Cited by 1
Gunster, J. L. B., Tramm, T., Machiels, M., Demaria, S., Formenti, S. C., Caluwé, A. D., Duane, F. K., Klein, J., Sur, D. G., Somaiah, N., et al. (2026) · The Lancet Oncology · doi:10.1016/s1470-2045(26)00255-x · Cited by 1
Tohidi, N., Manshadi, S. A. D., & Hajiabdolbaghi, M. (2023) · Virus Genes · doi:10.1007/s11262-023-02032-9 · Cited by 1
Covalent Bifunctional Molecules (CBMs): Achievements and Challenges
Xin, Y., Chen, F., You, Q., Wang, L., & Zhang, Q. (2025) · Medicinal Research Reviews · doi:10.1002/med.70011 · Cited by 1
Sex-dependent interferon signaling drives female-biased vulnerability in Alzheimer’s diseasePreprint
López-López, V., Iniesta, G., Galán-Ganga, M., Exposito-Coca, A., Bhojwani-Cabrera, A. M., Guillot-Fernández, M., Giralt, A., & López‐Atalaya, J. P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.22.671724 · Cited by 1
Integrative analyses of DNA methylase expression and related immune landscape in Prostate CancerPreprint
Zhang, J., Huang, C. M., & Wang, H. (2024) · Research Square · doi:10.21203/rs.3.rs-4188677/v1
Hsu, T.-W., Li, S., Ho, Y.-J., Zhang, X., Malik, I., Bessel, D., Ji, L., Edwards, C., Capistrano, K. J., Vougiouklakis, T., et al. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5265216
Shekfeh, M., Konaté, M. M., & Krushkal, J. (2025) · Human Genomics · doi:10.1186/s40246-025-00785-y
“TREX1 protein expression is increased in multiple tumors, and higher levels of its expression were associated with worse prognosis in patients with wild type p53, as p53 promotes TREX1 protein degradation [53].”
Efficacy analysis of targeted P53 therapy in solid tumors
Wang, P., & Wang, F. (2025) · Medical Oncology · doi:10.1007/s12032-025-02930-y
“On this basis, combined with excessive Mn 2 ⁺ , the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway can be restored to activate the innate immune response [64, 65].”
Yuan, M., Wo, D., Gong, Y., Lin, M. V., Ma, E., Zhu, W., & Ren, D. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157091
“In contrast, the knockdown of p53 has been shown to accelerate CT26 tumor growth [32], supporting its importance in tumor suppression.”
Su, G., Wang, J., Xu, P., Zhang, Y., Gao, Y., Xue, F., & Li, Z. (2025) · Scientific Reports · doi:10.1038/s41598-025-29846-x
Zheng, L., Wei, J., Li, X., Li, M., Xue, C., Chen, S., Wei, Q., Fan, S., Xiong, W., Zhou, M., et al. (2025) · Cancers · doi:10.3390/cancers17243950
Lin, B., & Lai, Y. (2025) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2025.108873
Ishani, K., Wangmo, D., Ali, A. M., Gates, T. J., Yan, Z., Gustafson, A. P., Boytim, E., Storey, K. L., Goffredo, P., Hwang, J., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.03.703597
Co-Transfected Plasmids Enhance Transient Expression of Reporter Genes
Shih-Yen, L., Yang, C.-H., Chan, Y.-R., Chao, Y.-T., Lai, M., & Li, H. (2026) · BioTech · doi:10.3390/biotech15010023
Chen, X., Hou, Y., Chen, X.-X., Zhou, Q., & Wang, X. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1766502
Modified hTERT treatment ameliorates pressure overload-induced heart failure
Zhao, Y., Bao, X., Xiong, W., Wan, X., Yu, Q., Wang, T., Chang, A. C. H., Liu, Y., Wang, Y., Shang, C., et al. (2026) · EBioMedicine · doi:10.1016/j.ebiom.2026.106203
“66,67 Cytosolic p53 has been shown to participate in cGAS-STING activation 68 but more work is warranted to elucidate the degree of p53-cGAS-STING contribution.”
Zhang, C., Cao, S., Zeng, G., Dong, Y., Li, H., Ma, X., Zhang, X., Li, Z., & Huang, Y. (2026) · Scientific Reports · doi:10.1038/s41598-026-44653-8
“Reports that wild-type p53 can enhance innate immune pathways suggest that functional reprogramming of mutant p53 by APR-246 may contribute to immune activation 40,41 .”
Wu, X., Li, Y., Ye, Z., & Li, J. (2026) · The FASEB Journal · doi:10.1096/fj.202600624r
“…profound genomic and chromosomal instability (CIN) characteristic of malignancy [38], which frequently culminates in the formation of micronuclei; the subsequent rupture of the micronuclear envelope releases genomic DNA into the cyto-plasm, serving as a persistent internal stimulus for cGAS [39].”
Self-citationACOX2 at the crossroads of peroxisomal metabolism, DNA damage sensing, and anticancer immunity
Zheng, M., Zhao, B., Chen, X., & Zhao, Y. (2026) · Gene · doi:10.1016/j.gene.2026.150232 · Cited by 1
Miao, J., Zhang, S., Wang, M., Li, Z., Lv, N., & Sun, M. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1789002
Yan, X., Shi, L., Wen, F., Luo, J., Hu, J., Gai, L., Zhu, X., Hou, Z., Li, Q., Zhao, J., et al. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.154263
Qu, H., Zhou, P., Yu, J., Deng, K., Zhou, Y., Wang, N., Chen, Y., & Xia, J. (2026) · IntechOpen eBooks · doi:10.5772/intechopen.1016269
Klaver, D., Gander, H., Frena, B., Martin, M., Amato, M., Richter, J., Pichler, R., & Thurnher, M. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00515-3
“Consistently, cGAS-STING signaling was strongly activated in TAM-like macrophages, aligning with p53-driven mPTP opening [63] and STING activation [54] linked to senescence and aging-related inflammation [14, 55].”
Zheng, K., Che, B., Cui, Y., Yang, H., Xiang, Y., Gao, Y., Liu, P., Mu, Z., Wang, J., Xa, Y., et al. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.07.031 · Cited by 1
Ghosh, S., Mukherjee, S., & Mukherjee, A. (2026) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6c00727
Wang, Q., Xu, H.-W., Shi, Y., Zhang, Y.-P., jun, J. B. J., Yue, D.-N., Zhao, W., Huang, J.-Q., Peng, X.-L., Yu, J.-M., et al. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1904206
“Given that cytoplasmic dsDNA sensing by cGAS triggers STING signaling pathway (20, 21), we next examined its capacity to induce STING pathway activation in NCI-H226 cells.”
Zuo, H., Gao, X., Wang, Y., Yan, Y., Ru, Y., Zhao, J., Chen, X., Zhang, Y., Ma, X., Liu, X., et al. (2026) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6c00753
Immune response to DNA and RNA: structural insights, molecular mechanisms, and therapeutic targeting
Xia, L., Wang, Y., Yan, X., & Zhang, H. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00537-x
Zhong, H., Zhang, L., Xu, X., Zhang, M., Yang, X., & Hu, L. (2026) · International Journal of Genomics · doi:10.1155/ijog/5475028
The Dynamic Alliance of p53 and Metabolism in the Tumor Microenvironment Shapes Tumor Evolution
Joruiz, S. M., Napoletano, F., Bertolio, R., & Sal, G. D. (2026) · BioEssays · doi:10.1002/bies.70175
“In addition, WT p53 promotes the degradation of TREX1, a DNA exonuclease, resulting in cytosolic dsDNA accumulation, which activates the innate immunity cGAS/STING pathway stimulating IFN-I production [70].”
Chakraborty, S., Mukherjee, S., Ghosh, S., Basak, U., Mukherjee, S., Adhikary, A., Sa, G., & Das, T. (2026) · APOPTOSIS · doi:10.1007/s10495-026-02409-9
Suppressed cGAS–STING DNA Sensing Drives Immune Evasion in Anaplastic Thyroid Cancer
Zhu, X.-G., Acharya, M., Hwang, E., Wong, N. W., Nilubol, N., & Cheng, S.-Y. (2026) · Thyroid · doi:10.1177/10507256261481666
“37,38 In both the RU3 and orthotopic mouse models, the Trp53 gene is deleted.”
The Role of cGAS-STING-Driven PANoptosis in Neurodegenerative Diseases and Therapeutic Prospects
Hou, X., & Yu, W. (2026) · Cells · doi:10.3390/cells15181631
“WTp53 activates TBK1 independently of MAVS (mitochondrial antiviral signaling protein), indicating its specific targeting of DNA-sensing pathways [26].”
Liu, H., Yang, B., Chen, S., Li, Y., Zhang, Y., Huang, Y., Xing, J., Liu, H., Jiang, S., & Mo, R. (2026) · Nano Letters · doi:10.1021/acs.nanolett.6c02802
Yan, J., Zhou, T., Shi, S., Mao, G., Xu, J., Zhang, Y., Zhang, Y., Sun, H., Wang, Y., Wang, X., et al. (2026) · Cell · doi:10.1016/j.cell.2026.09.031 · Cited by 1
STING as a proton channel: Multifaceted roles in immunity and lysosomal homeostasis
Wang, N., Li, Y., Ma, L., Li, Y.-L., Chen, G., & Zeng, B. (2026) · Genes & Diseases · doi:10.1016/j.gendis.2026.102529
Yan, X., Gai, L., Yang, J., Li, W., Zhu, X., Huang, H., Zhao, Y., Huang, Y., Chen, Y., Li, Q., et al. (2026) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2026.107083
Wu, J.-Y., Wang, P., Li, L.-R., Chen, S.-L., Zhao, T., Zhou, J.-Y., Zhang, X.-Y., Huang, Y.-L., Tan, C.-P., & Wu, T. (2026) · Chemical Engineering Journal · doi:10.1016/j.cej.2026.183540
Metadata
- Authors
- Ghosh, M., Saha, S., Li, J., Montrose, D. C., & Martinez, L. A.
- Affiliations
- Stony Brook University (US)
- Stony Brook Medicine (US)
- Corresponding author
- Martinez, Luis A.
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2023-01
- Volume
- 83
- Issue
- 2
- Pages
- 266-280.e6
- ISSN
- 1097-2765 (ISSN-L)
- PMC
- PMC9993620
- OpenAlex
- W4315705275
- Cited by
- 166
- References
- 60
- Citations by year
- 2026: 48 · 2025: 54 · 2024: 37 · 2023: 27
- FWCI
- 18.10
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- 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, 383 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)
- Locations
- Molecular Cell (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Stony Brook University
- National Institutes of Health
- National Cancer Institute (K22CA226033, R01CA166974)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Keywords
- TP53, p53, cGAS-STING pathway, cytosolic DNA sensing, TRIM24, type I interferon, IFNB1, tumor suppression, innate immunity, double-stranded DNA, ubiquitin ligase
- MeSH terms
- STING Protein, DNA, Immunity, Innate, Interferon Type I, Membrane Proteins, Nucleotidyltransferases, Signal Transduction, Tumor Suppressor Protein p53
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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