Transcriptional Cross Talk between NF-κB and p53

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WAF1, a potential mediator of p53 tumor suppression

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p53, the cellular gatekeeper for growth and division

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THE NF-κB AND IκB PROTEINS: New Discoveries and Insights

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Tumor suppressor p53 is a direct transcriptional activator of the human bax gene

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An Essential Role for NF-κB in Preventing TNF-α-Induced Cell Death

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TNF- and Cancer Therapy-Induced Apoptosis: Potentiation by Inhibition of NF-κB

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Suppression of TNF-α-Induced Apoptosis by NF-κB

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A model for p53-induced apoptosis

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Role of NF-kB, p53, and p21 in the Regulation of TNF-α Mediated Apoptosis of Lymphocytes

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ROS and RNS induced apoptosis through p53 and iNOS mediated pathway by a dibasic hydroxamic acid molecule in leukemia cells

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HEY1 functions are regulated by its phosphorylation at Ser-68

López-Mateo, I., Arruabarrena-Aristorena, A., Artaza‐Irigaray, C., López, J. A., Calvo, E., & Belandia, B. (2016) · Bioscience Reports · doi:10.1042/bsr20160123 · Cited by 20

NF-κB p50 activation associated with immune dysregulation confers poorer survival for diffuse large B-cell lymphoma patients with wild-type p53

Cai, Q., Tu, M., Xu-Monette, Z. Y., Sun, R., Manyam, G. C., Xu, X., Tzankov, A., Hsi, E. D., Møller, M. B., Medeiros, L. J., et al. (2017) · Modern Pathology · doi:10.1038/modpathol.2017.5 · Cited by 22

Transition of amyloid/mutant p53 from tumor suppressor to an oncogene and therapeutic approaches to ameliorate metastasis and cancer stemness

Sengupta, S., Ghufran, S. M., Khan, A. A., Biswas, S., & Roychoudhury, S. (2022) · Cancer Cell International · doi:10.1186/s12935-022-02831-4 · Cited by 20

Transcriptional activation of APAF1 by KAISO (ZBTB33) and p53 is attenuated by RelA/p65

Koh, D., An, H., Kim, M., Jeon, B., Choi, S., Hur, S. S., & Hur, M. (2015) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2015.07.008 · Cited by 20

Doxycycline Promotes Carcinogenesis & Metastasis via Chronic Inflammatory Pathway: An In Vivo Approach

Nanda, N., Dhawan, D. K., Bhatia, A., Mahmood, A., & Mahmood, S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151539 · Cited by 20

The ubiquitin‐proteasome system in cancer, a major player in DNA repair. Part 2: transcriptional regulation

Vlachostergios, P. J., Patrikidou, A., Daliani, D., & Papandreou, C. N. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00825.x · Cited by 22

Cross-Regulation of T Cell Growth Factor Expression by p53 and the Tax Oncogene

Chaudhry, S., Freebern, W. J., Smith, J. L., Butscher, W. G., Haggerty, C. M., & Gardner, K. L. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.12.6767 · Cited by 20

Phosphorylation of IGFBP-3 by Casein Kinase 2 Blocks Its Interaction with Hyaluronan, Enabling HA-CD44 Signaling Leading to Increased NSCLC Cell Survival and Cisplatin Resistance

Coleman, K.-L., Chiaramonti, M., Haddad, B., Ranzenberger, R., Henning, H., Khashali, H. A., Ray, R., Darweesh, B., Guthrie, J. W., Heyl, D., et al. (2023) · Cells · doi:10.3390/cells12030405 · Cited by 19

Antitumor mechanism of cannabidiol hidden behind cancer hallmarks

Yan, C., Li, Y., Liu, H., Chen, D., & Wu, J. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.188905 · Cited by 19

Co-expression of RelA/p65 and ACTN4 induces apoptosis in non-small lung carcinoma cells

Lomert, E. V., Turoverova, L. V., Kriger, D. V., Aksenov, N. D., Nikotina, A. D., Petukhov, A., Mittenberg, A. G., Panyushev, N. V., Георгиевич, Х. М., Volkov, K. V., et al. (2017) · Cell Cycle · doi:10.1080/15384101.2017.1417709 · Cited by 19

Differences in the Relative Abundance of ProBDNF and Mature BDNF in A549 and H1299 Human Lung Cancer Cell Media

Dorandish, S., Atali, S., Ray, R., Khashali, H. A., Coleman, K.-L., Guthrie, J. W., Heyl, D., & Evans, H. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137059 · Cited by 19

Activating Mas receptor protects human pulmonary microvascular endothelial cells against LPS‐induced apoptosis via the NF‐kB p65/P53 feedback pathways

Huang, W.-F., Cao, Y., Liu, Y., Feng, P., Shang, J., Zhang, Z., & Li, Y. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27951 · Cited by 19

The Large Subunit of Replication Factor C Interacts with the Histone Deacetylase, HDAC1

Anderson, L. A., & Perkins, N. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200513200 · Cited by 19

Context-dependent Pax-5 repression of a PU.1/NF-κB regulated reporter gene in B lineage cells

Linderson, Y., French, N. S., Neurath, M. F., & Pettersson, S. (2001) · Gene · doi:10.1016/s0378-1119(00)00546-1 · Cited by 19

Studies on modulation of the activity of tumor suppressor protein p53

Kadaja, L. (2004) · DSpace repository (University of Tartu) · Cited by 19

Effect of canonical NF-κB signaling pathway on the differentiation of rat dental epithelial stem cells

Liang, Y., Chen, G., Yang, Y., Li, Z., Chen, T., Sun, W., Yu, M., Pan, K., Guo, W., & Tian, W. (2019) · Stem Cell Research & Therapy · doi:10.1186/s13287-019-1252-7 · Cited by 18

NKX2-1-mediated p53 expression modulates lung adenocarcinoma progression via modulating IKKβ/NF-κB activation

Chen, P.-M., Wu, T., Cheng, Y., Chen, C., & Lee, H. (2015) · Oncotarget · doi:10.18632/oncotarget.3695 · Cited by 18

Hematopoietic Protection by Dexamethasone or Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF) in Patients Treated With Carboplatin and Ifosfamide

Rinehart, J. J., Keville, L., Neidhart, J., Wong, L., DiNunno, L., Kinney, P., Aberle, M., Tadlock, L., & Cloud, G. (2003) · American Journal of Clinical Oncology · doi:10.1097/01.coc.0000027268.23258.7d · Cited by 18

Increased NF-κB DNA binding but not transcriptional activity during apoptosis induced by the COX-2-selective inhibitor NS-398 in colorectal carcinoma cells

Smartt, H. J. M., Elder, D. J. E., Hicks, D. J., Williams, N., & Paraskeva, C. (2003) · British Journal of Cancer · doi:10.1038/sj.bjc.6601266 · Cited by 18

Cell Nucleus in Context

Lelièvre, S. A., Bisseil, M. J., & Pujuguet, P. (2000) · Critical Reviews in Eukaryotic Gene Expression · doi:10.1615/critreveukargeneexpr.v10.i1.30 · Cited by 18

Antisense Evidence for Nuclear Factor-κB–Dependent Embryopathies Initiated by Phenytoin-Enhanced Oxidative Stress

Kennedy, J., Mémet, S., & Wells, P. G. (2004) · Molecular Pharmacology · doi:10.1016/s0026-895x(24)05622-0 · Cited by 18

Secretory leukocyte protease inhibitor suppresses HPV E6-expressing HNSCC progression by mediating NF-κB and Akt pathways

Jin, Y., Li, Y., Wang, X., & Yang, Y. (2019) · Cancer Cell International · doi:10.1186/s12935-019-0942-7 · Cited by 17

Inflammation-associated genomic instability in cancer

Pua, K. H., Chew, C. L., Lane, D. P., & Tergaonkar, V. (2019) · Genome Instability & Disease · doi:10.1007/s42764-019-00006-6 · Cited by 17

Coactivator requirements for p53‐dependent transcription in the yeast Saccharomyces cerevisiae

Yousef, A. F., Xu, G. W., Mendez, M., Brandl, C. J., & Mymryk, J. S. (2007) · International Journal of Cancer · doi:10.1002/ijc.23174 · Cited by 17

TNFalpha-induced activation of NFkappaB protects against UV-induced apoptosis specifically in p53-proficient cells.

Szołtysek, K., Pietranek, K., Kalinowska, M., Pietrowska, M., Kimmel, M., & Widłak, P. (2008) · Acta Biochimica Polonica · doi:10.18388/abp.2008_3035 · Cited by 17

Effect of zinc(II) ions on the expression of pro- and anti-apoptotic factors in high-grade prostate carcinoma cells

Sztalmachová, M., Hlavna, M., Gumulec, J., Holubová, M., Babula, P., Balvan, J., Sochor, J., Tanhäuserová, V., Raudenská, M., Křížková, S., et al. (2012) · Oncology Reports · doi:10.3892/or.2012.1897 · Cited by 17

Role of peroxidases, thiols and Bak/Bax in tumor cell susceptibility to Cu[DEDTC]2

Viola-Rhenals, M., RIEBER, M. S., & Rieber, M. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.06.048 · Cited by 17

Prognostic Significance of theBIRC2-BIRC3Gene Signature in Head and Neck Squamous Cell Carcinoma

Lee, M. K., Noh, J. K., Woo, S. R., Kong, M., Lee, Y. C., Lee, J. W., Ko, S., & Eun, Y. (2022) · Cancer Genomics & Proteomics · doi:10.21873/cgp.20344 · Cited by 16

Diverse roles of UBE2S in cancer and therapy resistance: Biological functions and mechanisms

Zhang, M., Wang, J., Zhang, Z., Guo, Y., Lou, X., & Zhang, L. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e24465 · Cited by 16

p53 functions and cell lines: Have we learned the lessons from the past?

Millau, J., Mai, S., Bastien, N., & Drouin, R. (2010) · BioEssays · doi:10.1002/bies.200900160 · Cited by 16

A Bioactive Extract Rich in Triterpenic Acid and Polyphenols from Olea europaea Promotes Systemic Immunity and Protects Atlantic Salmon Smolts Against Furunculosis

Salomón, R., Furones, M. D., Reyes‐López, F. E., Tort, L., Firmino, J. P., Esteban, M. Á., Espinosa‐Ruíz, C., Quintela, J. C., Pinilla-Rosas, J. M., Vallejos‐Vidal, E., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.737601 · Cited by 16

Persistence of unrepaired DNA double strand breaks caused by inhibition of ATM does not lead to radio-sensitisation in the absence of NF-κB activation

Veuger, S. J., & Durkacz, B. W. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.11.005 · Cited by 16

P53, Cell Cycle Arrest and Apoptosis

Wang, S., & El‐Deiry, W. S. (2005) · Springer eBooks · doi:10.1007/978-1-4020-2922-6_6 · Cited by 17

Downstream Codons in the Retinoic Acid Receptor β-2 and β-4 mRNAs Initiate Translation of a Protein Isoform That Disrupts Retinoid-activated Transcription

Chen, L. I., Sommer, K. M., & Swisshelm, K. L. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m202717200 · Cited by 16

Sabarubicin- (MEN 10755) and paclitaxel show different kinetics in nuclear factor-kappaB (NF-kB) activation: effect of parthenolide on their cytotoxicity.

Bellarosa, D., Binaschi, M., Maggi, C. A., & Goso, C. (2005) · PubMed · Cited by 16

Olive Oil Improves While Trans Fatty Acids Further Aggravate the Hypomethylation of LINE-1 Retrotransposon DNA in an Environmental Carcinogen Model

Szabó, L. G., Molnár, R., Tomesz, A., Deutsch, A., Darago, R., Varjas, T., Ritter, Z., Szentpéteri, J. L., Andreidesz, K., Máthé, D., et al. (2022) · Nutrients · doi:10.3390/nu14040908 · Cited by 15

Sequential drug treatment targeting cell cycle and cell fate regulatory programs blocks non-genetic cancer evolution in acute lymphoblastic leukemia

Malyukova, A., Lahnalampi, M., Falqués, T., Pölönen, P., Sipola, M., Mehtonen, J., Teppo, S., Akopyan, K., Viiliäinen, J., Lohi, O., et al. (2024) · Genome biology · doi:10.1186/s13059-024-03260-4 · Cited by 15

p53 modulates NF-κB mediated epithelial-to-mesenchymal transition in head and neck squamous cell carcinoma

Lin, Y., Clair, J. M., Luo, J., Sharma, S. P., Dubinett, S. M., & John, M. A. S. (2015) · Oral Oncology · doi:10.1016/j.oraloncology.2015.07.006 · Cited by 15

Pulsed Electric Fields Alter Expression of NF-κB Promoter-Controlled Gene

Kavaliauskaitė, J., Kazlauskaitė, A., Lazutka, J. R., Mozoļevskis, G., & Stirkė, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010451 · Cited by 15

Parthenolide complements the cell death-inducing activity of doxorubicin in melanoma cells.

Woźniak, M., Szuławska‐Mroczek, A., Hartman, M. L., Nejc, D., & Czyż, M. (2013) · PubMed · Cited by 15

External zinc stimulates proliferation of tumor Hep-2 cells by active modulation of key signaling pathways

Rudolf, E., & Červinka, M. (2008) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2007.12.003 · Cited by 15

Up-regulation of NFκB-responsive gene expression by ΔNp73α in p53 null cells

Tanaka, Y., Ota, K., Kameoka, M., Itaya, A., & Yoshihara, K. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2005.12.013 · Cited by 15

p53 regulates the transcription of the anti-inflammatory molecule developmental endothelial locus-1 (Del-1)

Kim, H., Lee, S. H., Lee, M.-N., Oh, G. T., Choi, K., & Choi, E. Y. (2013) · Oncotarget · doi:10.18632/oncotarget.1318 · Cited by 15

Mutant p53 reactivator SLMP53-2 hinders ultraviolet B radiation-induced skin carcinogenesis

Loureiro, J. B., Ribeiro, R. S. R., Nazareth, N., Ferreira, T., Lopes, E. A., Gama, A., Machuqueiro, M., Alves, M. G., Marabini, L., Oliveira, P. A., et al. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.106026 · Cited by 14

Developmental endothelial locus-1 inhibits MIF production through suppression of NF-κB in macrophages

Lee, S., Kim, D.-Y., KANG, Y.-Y., Kim, H., JANG, J., LEE, M.-N., Oh, G. T., Kang, S., & Choi, E. Y. (2014) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2014.1645 · Cited by 14

Regulation of p53 and NF-κB transactivation activities by DGKζ in catalytic activity-dependent and -independent manners

Tanaka, T., Nakano, T., Hozumi, Y., Martelli, A. M., & Goto, K. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2021.118953 · Cited by 15

p300 expression is induced by oxygen deficiency and protects neuron cells from damage

Tan, X. L., Zhai, Y., Gao, W. X., Fan, Y. M., Liu, F. Y., Huang, Q. Y., & Gao, Y. Q. (2008) · Brain Research · doi:10.1016/j.brainres.2008.11.092 · Cited by 14

Pithecellobium dulce induces apoptosis and reduce tumor burden in experimental animals via regulating pro-inflammatory cytokines and anti-apoptotic gene expression

Dhanisha, S. S., Drishya, S., & Guruvayoorappan, C. (2022) · Food and Chemical Toxicology · doi:10.1016/j.fct.2022.112816 · Cited by 13

Regulation of CXCR4 gene expression in breast cancer cells under diverse stress conditions

Andreou, K. E., Rajendran, R., Krstic–Demonacos, M., & Demonacos, C. (2012) · International Journal of Oncology · doi:10.3892/ijo.2012.1643 · Cited by 13

Molecular Dynamics in Esophageal Adenocarcinoma: Who’s in Control?

Dang, T., & Chai, J. (2020) · Current Cancer Drug Targets · doi:10.2174/1568009620666200720011341 · Cited by 13

Urine-derived extracellular vesicle miRNAs as possible biomarkers for and mediators of necrotizing enterocolitis: A proof of concept study

Galley, J. D., Mar, P. K., Wang, Y., Han, R., Rajab, A., & Besner, G. E. (2021) · Journal of Pediatric Surgery · doi:10.1016/j.jpedsurg.2021.02.016 · Cited by 14

Cellular origin of ionizing radiation‐induced NF‐κB activationin vivoand role of NF‐κB in ionizing radiation‐induced lymphocyte apoptosis

Meng, A., Yu, T., Chen, G., Brown, S. A., Wang, Y., Thompson, J. S., & Zhou, D. (2003) · International Journal of Radiation Biology · doi:10.1080/09553000310001622814 · Cited by 13

Comparison of genotoxic versus nongenotoxic stabilization of p53 provides insight into parallel stress-responsive transcriptional networks

Catizone, A. N., Good, C. R., Alexander, K. A., Berger, S. L., & Sammons, M. A. (2019) · Cell Cycle · doi:10.1080/15384101.2019.1593643 · Cited by 12

Signaling through TLR5 mitigates lethal radiation damage by neutrophil-dependent release of MMP-9

Brackett, C. M., Greene, K. F., Aldrich, A., Trageser, N. H., Pal, S., Molodtsov, I. A., Kandar, B. M., Burdelya, L. G., Abrams, S. I., & Gudkov, A. V. (2021) · Cell Death Discovery · doi:10.1038/s41420-021-00642-6 · Cited by 12

Reduction of lithium induced interstitial fibrosis on co-administration with amiloride

Mehta, P. M., Gimenez, G., Walker, R. J., & Slatter, T. L. (2022) · Scientific Reports · doi:10.1038/s41598-022-18825-1 · Cited by 12

Diflovidazin damages the hematopoietic stem cells to zebrafish embryos via the TLR4/ NF-κB/ p53 pathway

Jia, K., Xiong, H., Yuan, W., Huang, L., Xu, J., Lu, C., Hu, Y., Huang, K., Luo, Q., Ma, J., et al. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.108672 · Cited by 12

Regulation of apoptosis in the female reproductive system

Vaskivuo, T. E. (2002) · Cited by 12

NF-κB prevents cells from undergoing Cr(VI)-induced apoptosis

Wang, S., Chen, F., Zhang, Z., Shi, X., Jiang, B., & Luo, J. (2003) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000007269.74532.98 · Cited by 12

ROCK2/rasHa co-operation induces malignant conversion via p53 loss, elevated NF-κB and tenascin C-associated rigidity, but p21 inhibits ROCK2/NF-κB-mediated progression

Masre, S. F., Rath, N., Olson, M. F., & Greenhalgh, D. A. (2016) · Oncogene · doi:10.1038/onc.2016.402 · Cited by 12

Regulation of Vascular Endothelial Growth Factor Signaling by Nicotine in a Manner Dependent on Acetylcholine-and/or β-Adrenergic-Receptors in Human Lung Cancer Cells

Khashali, H. A., Darweesh, B., Ray, R., Haddad, B., Wozniak, C., Ranzenberger, R., Goel, S., Khalil, J., Guthrie, J. W., Heyl, D., et al. (2023) · Cancers · doi:10.3390/cancers15235500 · Cited by 11

TAK1 signaling regulates p53 through a mechanism involving ribosomal stress

Zonneville, J., Wong, V., Limoge, M., Nikiforov, M. A., & Bakin, A. V. (2020) · Scientific Reports · doi:10.1038/s41598-020-59340-5 · Cited by 12

Some properties of the signals involved in unirradiated zebrafish embryos rescuing α-particle irradiated zebrafish embryos

Kong, E. Y., Choi, V. W. Y., Cheng, S. H., & Yu, K. N. (2014) · International Journal of Radiation Biology · doi:10.3109/09553002.2014.932031 · Cited by 11

Cytoplasmic p21 induced by p65 prevents doxorubicin-induced cell death in pancreatic carcinoma cell line

Zhou, Y., Li, G., Ji, Y., Liu, C., Zhu, J., & Lu, Y. (2012) · Journal of Biomedical Science · doi:10.1186/1423-0127-19-15 · Cited by 11

Inflammation-Related Pancreatic Carcinogenesis

Dai, J., Jiang, M., Wang, X., & Tian, L. (2017) · Pancreas · doi:10.1097/mpa.0000000000000886 · Cited by 11

Low‐dose rotenone exposure induces early senescence leading to late apoptotic signaling cascade in human trabecular meshwork (HTM) cell line: An in vitro glaucoma model

Maurya, N., Agarwal, N. R., & Ghosh, I. (2015) · Cell Biology International · doi:10.1002/cbin.10561 · Cited by 11

Disulfiram and metformin combination anticancer effect reversible partly by antioxidant nitroglycerin and completely by NF-κB activator mebendazole in hamster fibrosarcoma

Popović, K. J., Popović, D. J., Miljković, D., Popović, J. K., Lalošević, D., Poša, M., & Čapo, I. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112168 · Cited by 10

Sustained activation of NF-κB through constitutively active IKKβ leads to senescence bypass in murine dermal fibroblasts

Harada, M., Su-Harada, K., Kimura, T., Ono, K., & Ashida, N. (2024) · Cell Cycle · doi:10.1080/15384101.2024.2325802 · Cited by 10

Regulation of matrix metalloproteinase-9 transcription in squamous cell carcinoma of uterine cervix: the role of human papillomavirus gene E2 expression and activation of transcription factor NF-κB

Gasparian, A. V., Fedorova, M. D., & Kisseljov, F. L. (2007) · Biochemistry (Moscow) · doi:10.1134/s0006297907080068 · Cited by 10

MAFIP is a tumor suppressor in cervical cancer that inhibits activation of the nuclear factor‐kappa B pathway

Li, Y., Yu, Y., Zhang, Y., Zhou, Y., Li, C., Zhu, J., Yuan, H., & Lü, H. (2011) · Cancer Science · doi:10.1111/j.1349-7006.2011.02061.x · Cited by 10

Cellular response of blood and hepatic tissue to gamma irradiation

Mohamed, M. A., Saeid, A. A. E., & Ahmed, M. A. (2015) · Journal of Radiation Research and Applied Sciences · doi:10.1016/j.jrras.2015.12.001 · Cited by 10

Nuclear factor κB signaling revisited: Its role in skeletal muscle and exercise

Ji, L. L. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.02.013 · Cited by 9

Inflammatory signaling in the pathogenesis of acute myeloid leukemia

Baumann, A., & Ellegast, J. M. (2025) · HemaSphere · doi:10.1002/hem3.70188 · Cited by 9

NF-κB/p52 augments ETS1 binding genome-wide to promote glioma progression

Sim, N., & Li, Y. (2023) · Communications Biology · doi:10.1038/s42003-023-04821-2 · Cited by 9

Constitutive IL-8 expression in cancer cells is associated with mutation of p53.

Hidaka, H., Ishiko, T., Ishikawa, S., Ikeda, O., Mita, S., Iwamura, T., Chijiiwa, K., & Ogawa, M. (2005) · PubMed · Cited by 9

An endoribonuclease-based feedforward controller for decoupling resource-limited genetic modules in mammalian cellsPreprint

Jones, R. D., Qian, Y., Siciliano, V., DiAndreth, B., Huh, J. H., Weiss, R., & Vecchio, D. D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/867028 · Cited by 9

Gemcitabine therapeutically disrupts essential SIRT1-mediated p53 repression in atypical teratoid/rhabdoid tumors

Metselaar, D. S., Meel, M. H., Goulding, J. R., du Chatinier, A., Rigamonti, L., Waranecki, P., Geisemeyer, N., de Gooijer, M. C., Breur, M., Köster, J., et al. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101700 · Cited by 8

The Nuclear Factor-κB and p53 Pathways Function Independently in Primary Cells and Transformed Fibroblasts Responding to Genotoxic Damage

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Development of NIPAAm-PEG acrylate polymeric nanoparticles for co-delivery of paclitaxel with ellagic acid for the treatment of breast cancer

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