Transcriptional Cross Talk between NF-κB and p53

Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

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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

Baldwin, A. S. (1996) · Annual Review of Immunology · doi:10.1146/annurev.immunol.14.1.649 · Cited by 5,882

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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NF-kappaB antiapoptosis: induction of TRAF1 and TRAF2 and c-IAP1 and c-IAP2 to suppress caspase-8 activation.

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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

Polyak, K., Xia, Y., Zweier, J. L., Kinzler, K. W., & Vogelstein, B. (1997) · Nature · doi:10.1038/38525 · Cited by 2,500

IL-8 and p53 are inversely regulated through JNK, p38 and NF-κB p65 in HepG2 cells during an inflammatory response

Rasmussen, M. K., Iversen, L., Johansen, C., Finnemann, J., Olsen, L. S., Kragballe, K., & Gesser, B. (2008) · Inflammation Research · doi:10.1007/s00011-007-7220-1 · Cited by 37

Conjugated Linoleic Acids Can Change Phagocytosis of Human Monocytes/Macrophages by Reduction in Cox‐2 Expression

Stachowska, E., Baśkiewicz‐Masiuk, M., Dziedziejko, V., Adler, G., Bober, J., Machaliński, B., & Chlubek, D. (2007) · Lipids · doi:10.1007/s11745-007-3072-2 · Cited by 37

T-oligo Treatment Decreases Constitutive and UVB-induced COX-2 Levels through p53- and NFκB-dependent Repression of the COX-2 Promoter

Marwaha, V., Chen, Y., Helms, E., Arad, S., Inoue, H., Bord, E., Kishore, R., Sarkissian, R. D., Gilchrest, B. A., & Goukassian, D. A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503245200 · Cited by 37

The ubiquitin‐proteasome system in cancer, a major player in DNA repair. Part 1: post‐translational regulation

Vlachostergios, P. J., Patrikidou, A., Daliani, D., & Papandreou, C. N. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00824.x · Cited by 36

Cylindrospermopsin induced transcriptional responses in human hepatoma HepG2 cells

Štraser, A., Filipič, M., & Žegura, B. (2013) · Toxicology in Vitro · doi:10.1016/j.tiv.2013.05.012 · Cited by 35

Estradiol-mediated inhibition of DNMT1 decreases p53 expression to induce M2-macrophage polarization in lung cancer progression

Chen, Y.-C., Young, M.-J., Chang, H.-P., Liu, C.-Y., Lee, C.-C., Tseng, Y., Wang, Y., Chang, W., & Hung, J. (2022) · Oncogenesis · doi:10.1038/s41389-022-00397-4 · Cited by 35

p53 modulates the activity of the GLI1 oncogene through interactions with the shared coactivator TAF9

Yoon, J. W., Lamm, M. L. G., Iannaccone, S., Higashiyama, N., Leong, K.-F., Iannaccone, P. M., & Walterhouse, D. O. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.06.006 · Cited by 35

Embryonic mouse submandibular salivary gland morphogenesis and the TNF/TNF-R1 signal transduction pathway

Melnick, M., Chen, H., Zhou, Y., & Jaskoll, T. F. (2001) · The Anatomical Record · doi:10.1002/1097-0185(20010301)262:3 · Cited by 35

Reciprocal regulation of p53 and NF-κB by diacylglycerol kinase ζ

Tanaka, T., Tsuchiya, R., Hozumi, Y., Nakano, T., Okada, M., & Goto, K. (2015) · Advances in Biological Regulation · doi:10.1016/j.jbior.2015.09.009 · Cited by 34

Wip1 sensitizes p53-negative tumors to apoptosis by regulating the Bax/Bcl-xLratio

Goloudina, A. R., Mazur, S. J., Appella, E., Garrido, C., & Demidov, O. N. (2012) · Cell Cycle · doi:10.4161/cc.19901 · Cited by 37

A Brief look at antitumor effects of doxycycline in the treatment of colorectal cancer and combination therapies

Ghasemi, K., & Ghasemi, K. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174593 · Cited by 34

p53/NF-kB Balance in SARS-CoV-2 Infection: From OMICs, Genomics and Pharmacogenomics Insights to Tailored Therapeutic Perspectives (COVIDomics)

Milani, D., Caruso, L., Zauli, E., Owaifeer, A. M. A., Secchiero, P., Zauli, G., Gemmati, D., & Tisato, V. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.871583 · Cited by 37

NF-kappaB function in the human myometrium during pregnancy and parturition.

Cookson, V. J., & Chapman, N. (2010) · PubMed · doi:10.14670/hh-25.945 · Cited by 35

Repression of Dmp1 and Arf transcription by anthracyclins: critical roles of the NF-κB subunit p65

Taneja, P., Mallakin, A., Matise, L. A., Frazier, D. P., Choudhary, M., & Inoue, K. (2007) · Oncogene · doi:10.1038/sj.onc.1210568 · Cited by 34

Physical Interaction and Mutual Transrepression between CCAAT/Enhancer-binding Protein β and the p53 Tumor Suppressor

Schneider‐Merck, T., Pohnke, Y., Kempf, R., Christian, M., Brosens, J. J., & Gellersen, B. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503459200 · Cited by 34

Global Analysis of CPEBs Reveals Sequential and Non-Redundant Functions in Mitotic Cell Cycle

Giangarrà, V., Igea, A., Castellazzi, C. L., Bava, F.-A., & Méndez, R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138794 · Cited by 35

Neuronal κB-binding Factors Consist of Sp1-related Proteins

Mao, X. R., Moerman, A., & Barger, S. W. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204292200 · Cited by 35

Downregulation of diacylglycerol kinase ζ enhances activation of cytokine-induced NF-κB signaling pathway

Tsuchiya, R., Tanaka, T., Hozumi, Y., Nakano, T., Okada, M., Topham, M. K., Iino, M., & Goto, K. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2014.11.011 · Cited by 33

RRAD, IL4I1, CDKN1A, and SERPINE1 genes are potentially co-regulated by NF-κB and p53 transcription factors in cells exposed to high doses of ionizing radiation

Szołtysek, K., Janus, P., Zając, G., Stokowy, T., Walaszczyk, A., Widłak, W., Wojtaś, B., Gielniewski, B., Cockell, S., Perkins, N. D., et al. (2018) · BMC Genomics · doi:10.1186/s12864-018-5211-y · Cited by 35

TGF‐β1–p53 cooperativity regulates a profibrotic genomic program in the kidney: molecular mechanisms and clinical implications

Higgins, C. E., Tang, J., Mian, B. M., Higgins, S. P., Gifford, C. C., Conti, D. J., Meldrum, K. K., Samarakoon, R., & Higgins, P. J. (2019) · The FASEB Journal · doi:10.1096/fj.201900943r · Cited by 34

Targeting codon 158 p53-mutant cancers via the induction of p53 acetylation

Kong, L. R., Ong, R., Tan, T. Z., Salleh, N. A. B. M., Thangavelu, M. T., Chan, J. V., Koh, L. Y. J., Periyasamy, G., Lau, J. A., Le, T. B. U., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15608-y · Cited by 34

The functional genomic response of developing embryonic submandibular glands to NF-kappaB inhibition

Melnick, M., Chen, H., Zhou, Y. M., & Jaskoll, T. F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-15 · Cited by 33

UBE2S activates NF-κB signaling by binding with IκBα and promotes metastasis of lung adenocarcinoma cells

Ho, J.-Y., Lu, H., Cheng, H.-H., Kuo, Y.-C., Lee, Y.-L. A., & Cheng, C. (2021) · Cellular Oncology · doi:10.1007/s13402-021-00639-4 · Cited by 32

Review: NF-kB activation in canine cancer

Schlein, L. J., & Thamm, D. H. (2022) · Veterinary Pathology · doi:10.1177/03009858221092017 · Cited by 32

Synthesis and Mechanistic Studies of a Novel Homoisoflavanone Inhibitor of Endothelial Cell Growth

Basavarajappa, H. D., Lee, B., Fei, X., Lim, D., Callaghan, B., Mund, J. A., Case, J., Gangaraju, R., Seo, S., & Corson, T. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0095694 · Cited by 32

TAT-mediated intracellular delivery of NPM-derived peptide induces apoptosis in leukemic cells and suppresses leukemogenesis in mice

Zhou, Y., Du, W., Koretsky, T., Bagby, G. C., & Pang, Q. (2008) · Blood · doi:10.1182/blood-2007-12-130211 · Cited by 32

Crosstalk between the NF‐κB activating IKK‐complex and the CSN signalosome

Orel, L., Neumeier, H., Hochrainer, K., Binder, B. R., & Schmid, J. A. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00866.x · Cited by 32

Secretory leukocyte protease inhibitor (SLPI) in cancer pathophysiology: Mechanisms of action and clinical implications

Zhang, X., Liu, S. S., Ma, J., & Qu, W. (2023) · Pathology - Research and Practice · doi:10.1016/j.prp.2023.154633 · Cited by 32

The molecular mechanism of NF-κB dysregulation across different subtypes of renal cell carcinoma

Jayab, N. N. A., Abed, A., Talaat, I. M., & Hamoudi, R. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.07.030 · Cited by 31

Long non-coding RNA 00607 as a tumor suppressor by modulating NF-κB p65/p53 signaling axis in hepatocellular carcinoma

Sun, Q., Hu, B., Fu, P., Tang, W., Zhang, X., Zhan, H., Sun, C., He, Y., Song, K., Xiao, Y., et al. (2018) · Carcinogenesis · doi:10.1093/carcin/bgy113 · Cited by 31

Effects of Acupuncture on Oxidative Stress Amelioration via Nrf2/ARE-Related Pathways in Alzheimer and Parkinson Diseases

Huang, T.-I., & Hsieh, C. (2021) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2021/6624976 · Cited by 31

Nuclear Factor-κB Regulates Inflammatory Cell Apoptosis and Phagocytosis in Rat Carrageenin-Sponge Implant Model

Maiuri, M. C., TAJANA, G., Iuvone, T., Stefano, D. D., Mele, G., Ribecco, M. T. S., Cinelli, M. P., Romano, M. F., Turco, M. C., & Carnuccio, R. (2004) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63280-4 · Cited by 31

Repression of Smad‐dependent transforming growth factor‐β signaling by Epstein‐Barr virus latent membrane protein 1 through nuclear factor‐κB

Mori, N., Morishita, M., Tsukazaki, T., & Yamamoto, N. (2003) · International Journal of Cancer · doi:10.1002/ijc.11146 · Cited by 31

Computational Reconstruction of NFκB Pathway Interaction Mechanisms during Prostate Cancer

Börnigen, D., Tyekucheva, S., Wang, X., Rider, J. R., Lee, G. M., Mucci, L. A., Sweeney, C. J., & Huttenhower, C. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004820 · Cited by 30

The tumour suppressor gene p53 modulates the severity of antigen-induced arthritis and the systemic immune response

Leech, M. T., Xue, J. R., Dacumos, A., Hall, P., Santos, L. L., Yang, Y. H., Li, M., Kitching, A. R., & Morand, E. F. (2008) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2008.03629.x · Cited by 30

Current overview of functions of FoxO proteins, with special regards to cellular homeostasis, cell response to stress, as well as inflammation and aging

Wątroba, M., Maślińska, D., & Maśliński, S. (2012) · Advances in Medical Sciences · doi:10.2478/v10039-012-0039-1 · Cited by 30

Nuclear factor-κB as a predictor of treatment response in breast cancer

Garg, A. K., Hortobágyi, G. N., Aggarwal, B. B., Şahin, A. A., & Buchholz, T. A. (2003) · Current Opinion in Oncology · doi:10.1097/00001622-200311000-00001 · Cited by 30

Plant polyphenols attenuate hepatic injury after hemorrhage/resuscitation by inhibition of apoptosis, oxidative stress, and inflammation via NF-kappaB in rats

Relja, B., Töttel, E., Breig, L., Henrich, D. M., Schneider, H., Marzi, İ., & Lehnert, M. (2011) · European Journal of Nutrition · doi:10.1007/s00394-011-0216-1 · Cited by 30

Characterization and Role of p53 Family Members in the Symbiont-Induced Morphogenesis of theEuprymna scolopesLight Organ

Goodson, M. S., Crookes‐Goodson, W. J., Kimbell, J. R., & McFall‐Ngai, M. (2006) · Biological Bulletin · doi:10.2307/4134573 · Cited by 31

Neurokinin-1 receptor (NK1R) inhibition sensitizes APL cells to anti-tumor effect of arsenic trioxide via restriction of NF-κB axis: Shedding new light on resistance to Aprepitant

Bashash, D., Safaroghli‐Azar, A., Bayati, S., Razani, E., Pourbagheri‐Sigaroodi, A., Gharehbaghian, A., Momeny, M., Sanjadi, M., Rezaei–Tavirani, M., & Ghaffari, S. H. (2018) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2018.08.010 · Cited by 30

Isosilybin A induces apoptosis in human prostate cancer cells via targeting Akt, NF‐κB, and androgen receptor signaling

Deep, G., Gangar, S. C., Oberlies, N. H., Kroll, D. J., & Agarwal, R. (2010) · Molecular Carcinogenesis · doi:10.1002/mc.20670 · Cited by 30

Identification of cytokine-induced nuclear factor-kappaB target genes in ovarian and breast cancer cells

Deregowski, V., Delhalle, S., Benoît, V., Bours, V., & Merville, M. (2002) · Biochemical Pharmacology · doi:10.1016/s0006-2952(02)01151-6 · Cited by 30

Presence of Insulin-Like Growth Factor Binding Proteins Correlates With Tumor-Promoting Effects of Matrix Metalloproteinase 9 in Breast Cancer

Park, J.-H., Rasch, M. G., Qiu, J., Lund, I. K., & Egeblad, M. (2015) · Neoplasia · doi:10.1016/j.neo.2015.04.003 · Cited by 29

Effects of Mycoplasmas on the Host Cell Signaling Pathways

Borchsenius, S. N., Vishnyakov, I. E., Chernova, O. A., Chernov, V. M., & Barlev, N. A. (2020) · Pathogens · doi:10.3390/pathogens9040308 · Cited by 29

Nuclear factor-kappaB protects the liver against genotoxic stress and functions independently of p53.

Lavon, I., Pikarsky, E., Gutkovich, E., Goldberg, I., Bar, J., Oren, M., & Ben‐Neriah, Y. (2003) · PubMed · Cited by 29

p53 regulates cyclophosphamide teratogenesis by controlling caspases 3, 8, 9 activation and NF-κB DNA binding

Pekar, O., Molotski, N., Savion, S., Fein, A., Toder, V., & Torchinsky, A. M. (2007) · Reproduction · doi:10.1530/rep-07-0086 · Cited by 29

Arnicolide D exerts anti-melanoma effects and inhibits the NF-κB pathway

Zhu, P., Zheng, Z., Fu, X., Li, J., Yin, C., Chou, J., Wang, Y., Liu, Y., Chen, Y., Bai, J., et al. (2019) · Phytomedicine · doi:10.1016/j.phymed.2019.153065 · Cited by 28

Transcriptional regulation of microRNA-100, −146a, and −150 genes by p53 and NFκB p65/RelA in mouse striatal STHdhQ7/ HdhQ7cells and human cervical carcinoma HeLa cells

Ghose, J., & Bhattacharyya, N. P. (2015) · RNA Biology · doi:10.1080/15476286.2015.1014288 · Cited by 28

Inflammation and insulin resistance exert dual effects on adipose tissue tumor protein 53 expression

Ortega, F. J., Moreno‐Navarrete, J. M., Mayas, D., Sérino, M., Rodríguez‐Hermosa, J. I., Ricart, W., Luche, É., Burcelin, R., Tinahones, F. J., Frühbeck, G., et al. (2013) · International Journal of Obesity · doi:10.1038/ijo.2013.163 · Cited by 31

Tetrahydroanthraquinone Derivative (±)-4-Deoxyaustrocortilutein Induces Cell Cycle Arrest and Apoptosis in Melanoma Cells via Upregulation of p21 and p53 and Downregulation of NF-kappaB

Genov, M. N., Kreiseder, B., Nagl, M., Drucker, E., Wiederstein, M., Muellauer, B., Krebs, J., Grohmann, T., Pretsch, D., Baumann, K., et al. (2016) · Journal of Cancer · doi:10.7150/jca.13614 · Cited by 28

Dual role of TMS1/ASC in death receptor signaling

Parsons, M. J., & Vertino, P. M. (2006) · Oncogene · doi:10.1038/sj.onc.1209684 · Cited by 28

Mechanisms of Organoselenium Compounds in Chemoprevention: Effects on Transcription Factor-DNA Binding

Youn, B. W., Fiala, E. S., & Sohn, O. S. (2001) · Nutrition and Cancer · doi:10.1207/s15327914nc401_7 · Cited by 28

Down-regulation of nuclear factor kappaB is required for p53-dependent apoptosis in X-ray-irradiated mouse lymphoma cells and thymocytes.

Kawai, H., Yamada, Y., Tatsuka, M., Niwa, O., Yamamoto, K., & Suzuki, F. (1999) · PubMed · Cited by 28

Cooperative interactions between p53 and NFκB enhance cell plasticity

Bisio, A., Zámborszky, J., Zaccara, S., Lion, M., Tebaldi, T., Sharma, V., Raimondi, I., Alessandrini, F., Ciribilli, Y., & Inga, A. (2014) · Oncotarget · doi:10.18632/oncotarget.2545 · Cited by 27

Effects of mycoplasma infection on the host organism response via p53/NF‐κB signaling

Borchsenius, S. N., Daks, A. A., Fedorova, O., Chernova, O. A., & Barlev, N. A. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26781 · Cited by 27

mot-2–Mediated Cross Talk between Nuclear Factor-κB and p53 Is Involved in Arsenite-Induced Tumorigenesis of Human Embryo Lung Fibroblast Cells

Li, Y., Xu, Y., Ling, M., Yang, Y., Wang, S., Li, Z., Zhou, J., Wang, X., & Liu, Q. (2010) · Environmental Health Perspectives · doi:10.1289/ehp.0901677 · Cited by 27

Endogenous Inhibitors of Nuclear Factor-κB, An Opportunity for Cancer Control

Chen, F. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-2096 · Cited by 27

Targeting p53 for immune modulation: Exploring its functions in tumor immunity and inflammation

Wu, H. H., Leng, S., Eisenstat, D. D., Sergi, C. M., & Leng, R. P. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.217614 · Cited by 27

Cross‐validation of Murine UV Signal Transduction Pathways in Human Skin†

Einspahr, J. G., Bowden, G. T., Alberts, D. S., McKenzie, N. E., Saboda, K., Warneke, J. A., Salasche, S. J., Ranger‐Moore, J., Curiel‐Lewandrowski, C. N., Nagle, R. B., et al. (2008) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2007.00287.x · Cited by 26

Regulation of RelA (p65) Function by the Large Subunit of Replication Factor C

Anderson, L. A., & Perkins, N. D. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.2.721-732.2003 · Cited by 26

Multiple Domains of Ruk/CIN85/SETA/CD2BP3 are Involved in Interaction with p85α Regulatory Subunit of PI 3-kinase

Borthwick, E. B., Korobko, I. V., Luke, C. T., Drel, V. R., Fedyshyn, Y., Ninkina, N. N., Дробот, Л. Б., & Buchman, V. L. (2004) · Journal of Molecular Biology · doi:10.1016/j.jmb.2004.08.075 · Cited by 26

NS5ATP9 gene regulated by NF-κB signal pathway

Li, K., Ma, Q., Shi, L., Dang, C., Yuan, H., Wang, Q., Li, Y., Fan, W., Zhang, L., & Cheng, J. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.08.005 · Cited by 25

Prostate cancer cells hyper-activate CXCR6 signaling by cleaving CXCL16 to overcome effect of docetaxel

Kapur, N., Mir, H., Sonpavde, G., Jain, S. R., Bae, S., Lillard, J. W., & Singh, S. (2019) · Cancer Letters · doi:10.1016/j.canlet.2019.04.001 · Cited by 26

Identification of two p53 isoforms from Litopenaeus vannamei and their interaction with NF-κB to induce distinct immune response

Li, H., Wang, S., Chen, Y., Lǚ, K., Yin, B., Li, S., He, J., & Li, C. (2017) · Scientific Reports · doi:10.1038/srep45821 · Cited by 25

Influence of Confounding Factors on Radiation Dose Estimation Using In Vivo Validated Transcriptional Biomarkers

Cruz-Garcia, L., O’Brien, G., Donovan, E. M., Gothard, L., Boyle, S., Laval, A., Testard, I., Ponge, L., Woźniak, G., Miszczyk, L., et al. (2018) · Health Physics · doi:10.1097/hp.0000000000000844 · Cited by 25

The NF-κB Nucleolar Stress Response Pathway

Thoms, H. C., & Stark, L. A. (2021) · Biomedicines · doi:10.3390/biomedicines9091082 · Cited by 24

Insights into molecular docking and dynamics to reveal therapeutic potential of natural compounds against P53 protein

Malla, B. A., Ali, A., Maqbool, I., Dar, N. A., Ahmad, S. B., Alsaffar, R. M., & Rehman, M. U. (2022) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2022.2137241 · Cited by 24

Spatio-temporal protein dynamics in single living cells

Ankers, J., Spiller, D. G., White, M., & Harper, C. V. (2008) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2008.07.001 · Cited by 25

A novel form of the RelA nuclear factor κB subunit is induced by and forms a complex with the proto-oncogene c-Myc

Chapman, N., Webster, G., Gillespie, P. J., Wilson, B. J., Crouch, D. H., & Perkins, N. D. (2002) · Biochemical Journal · doi:10.1042/bj20020444 · Cited by 24

Histone acetyltransferase p300 is a coactivator for transcription factor REL and is C-terminally truncated in the human diffuse large B-cell lymphoma cell line RC-K8

Garbati, M. R., Alço, G., & Gilmore, T. D. (2009) · Cancer Letters · doi:10.1016/j.canlet.2009.10.018 · Cited by 24

Sulphur alters NFκB-p300 cross-talk in favour of p53–p300 to induce apoptosis in non-small cell lung carcinoma

Saha, S., Bhattacharjee, P., Guha, D., Kajal, K., Khan, P., Chakraborty, S., Mukherjee, S., Paul, S., Manchanda, R. K., Khurana, A. K., et al. (2015) · International Journal of Oncology · doi:10.3892/ijo.2015.3061 · Cited by 23

Evaluating microRNA profiles reveals discriminative responses following genotoxic or non-genotoxic carcinogen exposure in primary mouse hepatocytes

Rieswijk, L., Brauers, K. J. J., Coonen, M. L. J., Breda, S. G. J. V., Jennen, D. G. J., & Kleinjans, J. C. S. (2015) · Mutagenesis · doi:10.1093/mutage/gev036 · Cited by 23

A novel mechanism for inhibition of lipopolysaccharide-induced proinflammatory cytokine production by valproic acid

Jambalganiin, U., Tsolmongyn, B., Koide, N., Odkhuu, E., Naiki, Y., Komatsu, T., Yoshida, T., & Yokochi, T. (2014) · International Immunopharmacology · doi:10.1016/j.intimp.2014.02.032 · Cited by 23

Loss of IKKβ activity increases p53 stability and p21 expression leading to cell cycle arrest and apoptosis

Yang, P., Huang, W., Lin, Y., Huang, W., Wu, H., Chen, W., Chang, Y., Chou, C., Tzeng, C., Chen, Y., et al. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00712.x · Cited by 24

Molecular changes induced by the curcumin analogue D6 in human melanoma cells

Rozzo, C., Fanciulli, M., Fraumene, C., Corrias, A., Cubeddu, T., Sassu, I., Cossu, S., Nieddu, V., Galleri, G., Azara, E., et al. (2013) · Molecular Cancer · doi:10.1186/1476-4598-12-37 · Cited by 23

Regulation of the leucocyte chemoattractant receptor FPR in glioblastoma cells by cell differentiation

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SHP-2 phosphatase contributes to KRAS-driven intestinal oncogenesis but prevents colitis-associated cancer development

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