Loss of p63 and its microRNA-205 target results in enhanced cell migration and metastasis in prostate cancer

The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1

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Integrative Genomic Profiling of Human Prostate Cancer

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p63, a p53 Homolog at 3q27–29, Encodes Multiple Products with Transactivating, Death-Inducing, and Dominant-Negative Activities

Yang, A., Kaghad, M., Wang, Y., Gillett, E. S., Fleming, M. D., Dötsch, V., Andrews, N. C., Caput, D., & McKeon, F. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80275-0 · Cited by 2,118

Gain of function of a p53 hot spot mutation in a mouse model of Li-Fraumeni syndrome

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Epithelial-Mesenchymal Transition in Breast Cancer Relates to the Basal-like Phenotype

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Mutant p53 drives invasion by promoting integrin recycling

Muller, P. A. J., Caswell, P. T., Doyle, B., Iwanicki, M. P., Tan, E. H., Karim, S., Lukashchuk, N., Gillespie, D. A., Ludwig, R. L., Gosselin, P., et al. (2009) · Cell · doi:10.1016/j.cell.2009.11.026 · Cited by 796

A Mutant-p53/Smad Complex Opposes p63 to Empower TGFβ-Induced Metastasis

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MicroRNAs as regulators of epithelial-mesenchymal transition

Gregory, P. A., Bracken, C. P., Bert, A. G., & Goodall, G. J. (2008) · Cell Cycle · doi:10.4161/cc.7.20.6851 · Cited by 521

Tumor predisposition in mice mutant for p63 and p73: Evidence for broader tumor suppressor functions for the p53 family

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MicroRNA expression profiling of human metastatic cancers identifies cancer gene targets

Baffa, R., Fassan, M., Volinia, S., O’Hara, B. J., Liu, C., Palazzo, J., Gardiman, M. P., Rugge, M., Gomella, L. G., Croce, C. M., et al. (2009) · The Journal of Pathology · doi:10.1002/path.2586 · Cited by 481

Emerging from the shade of p53 mutants: N-terminally truncated variants of the p53 family in EMT signaling and cancer progression

Engelmann, D., & Pützer, B. M. (2014) · Science Signaling · doi:10.1126/scisignal.2005699 · Cited by 39

Functions of TAp63 and p53 in restraining the development of metastatic cancer

Tan, E. H., Morton, J. P., Timpson, P., Tucci, P., Melino, G., Flores, E. R., Sansom, O. J., Vousden, K. H., & Muller, P. A. J. (2013) · Oncogene · doi:10.1038/onc.2013.287 · Cited by 39

The diverse oncogenic and tumour suppressor roles of p63 and p73 in cancer: a review by cancer site.

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Downregulation of miR-205 in migrating epithelial tongue facilitates skin wound re-epithelialization by derepressing ITGA5

Wang, T., Zhao, N., Long, S., Ge, L., Wang, A., Sun, H., Ran, X., Zou, Z., Wang, J., & Su, Y. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.05.004 · Cited by 39

Five microRNAs in serum as potential biomarkers for prostate cancer risk assessment and therapeutic intervention

Guo, X., Han, T., Hu, P., Guo, X., Zhu, C., Wang, Y., & Chang, S. (2018) · International Urology and Nephrology · doi:10.1007/s11255-018-2009-4 · Cited by 39

microRNA Expression and Biogenesis in Cellular Response to Ionizing Radiation

Mao, A., Liu, Y., Zhang, H., Di, C., & Sun, C. (2014) · DNA and Cell Biology · doi:10.1089/dna.2014.2401 · Cited by 38

p63 Attenuates Epithelial to Mesenchymal Potential in an Experimental Prostate Cell Model

Olsen, J. R., Oyan, A. M., Rostad, K., Hellem, M. R., Liu, J., Li, L., Micklem, D., Haugen, H., Lorens, J. B., Rotter, V., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062547 · Cited by 38

Coronary artery calcifications predict long term cardiovascular events in non diabetic Caucasian hemodialysis patients

Noce, A., Canale, M. P., Capria, A., Rovella, V., Tesauro, M., Splendiani, G., Annicchiarico‐Petruzzelli, M., Manzuoli, M., Simonetti, G., & Daniele, N. D. (2015) · Aging · doi:10.18632/aging.100740 · Cited by 38

Deciphering the function of non-coding RNAs in prostate cancer

Ramalho-Carvalho, J., Fromm, B., Henrique, R., & Jerónimo, C. (2016) · Cancer and Metastasis Reviews · doi:10.1007/s10555-016-9628-y · Cited by 39

Mutant p53 stimulates cell invasion through an interaction with Rad21 in human ovarian cancer cells

Ahn, J., Kim, T. J., Lee, J. H., & Choi, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-08880-4 · Cited by 38

TP63 basal cells are indispensable during endoderm differentiation into proximal airway cells on acellular lung scaffolds

Bilodeau, C., Shojaie, S., Goltsis, O., Wang, J., Luo, D., Ackerley, C. A., Rogers, I. M., Cox, B., & Post, M. (2021) · npj Regenerative Medicine · doi:10.1038/s41536-021-00124-4 · Cited by 37

Metastatic Prostate Cancer

Sailer, V. (2017) · Molecular pathology library · doi:10.1007/978-3-319-64096-9_17 · Cited by 38

The Panel of 12 Cell-Free MicroRNAs as Potential Biomarkers in Prostate Neoplasms

Konoshenko, M. Y., Lekchnov, E. A., Bryzgunova, O. E., Zaporozhchenko, I. A., Yarmoschuk, S. V., Pashkovskaya, O. A., Pak, S. V., & Laktionov, P. P. (2020) · Diagnostics · doi:10.3390/diagnostics10010038 · Cited by 35

Loss of TP63 Promotes the Metastasis of Head and Neck Squamous Cell Carcinoma by Activating MAPK and STAT3 Signaling

Lakshmanachetty, S., Balaiya, V., High, W. A., & Koster, M. I. (2019) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-18-1355 · Cited by 35

Deciphering the significance of p53 mutant proteins

Butera, A., & Amelio, I. (2024) · Trends in Cell Biology · doi:10.1016/j.tcb.2024.06.003 · Cited by 36

MiR‐205 suppresses tumor growth, invasion, and epithelial‐mesenchymal transition by targeting SEMA4C in hepatocellular carcinoma

Lu, J., Lin, Y., Li, F., Ye, H., Zhou, R., Jin, Y., Li, B., Xiong, X., & Cheng, N.-S. (2018) · The FASEB Journal · doi:10.1096/fj.201800113r · Cited by 33

MicroRNA-205 suppresses the oral carcinoma oncogenic activity via down-regulation of Axin-2 in KB human oral cancer cell

Kim, J., Park, S.-Y., Lee, S. A., Park, M.-G., Yu, S., Lee, M., Park, M., Kim, S.-G., Oh, J., Lee, S., et al. (2013) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-013-1872-7 · Cited by 34

MiR-223-5p works as an oncomiR in vulvar carcinoma byTP63suppression

Maia, B. D. M., Rodrigues, I. S., Akagi, E. M., do Amaral, N. S., Ling, H. Y., Monroig-Bosque, P. D. C., Soares, F. A., Călin, G. A., & Rocha, R. M. (2016) · Oncotarget · doi:10.18632/oncotarget.10247 · Cited by 34

MicroRNA-205 suppresses the invasion and epithelial-mesenchymal transition of human gastric cancer cells

Xu, C., Li, M., Zhang, L., Bi, Y., Wang, P., Li, J., & Jiang, X. (2016) · Molecular Medicine Reports · doi:10.3892/mmr.2016.5118 · Cited by 32

A microRNA/Runx1/Runx2 network regulates prostate tumor progression from onset to adenocarcinoma in TRAMP mice

Farina, N. H., Zingiryan, A., Akech, J., Callahan, C. J., Lu, H., Stein, J. L., Languino, L. R., Stein, G. S., & Lian, J. B. (2016) · Oncotarget · doi:10.18632/oncotarget.11992 · Cited by 32

Mutant p53 exerts oncogenic effects through microRNAs and their target gene networks

Li, X. L., Jones, M. F., Subramanian, M., & Lal, A. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.03.054 · Cited by 33

Molecular dynamics of the full-length p53 monomer

Chillemi, G., Davidovich, P. B., D’Abramo, M., Mametnabiev, T. E., Garabadzhiu, A. V., Desideri, A., & Melino, G. (2013) · Cell Cycle · doi:10.4161/cc.26162 · Cited by 31

The tumor suppressive miR-200b subfamily is an ERG target gene in human prostate tumors

Zhang, Z., Lanz, R. B., Xiao, L., Wang, L., Hartig, S. M., Ittmann, M., Feng, Q. F., & He, B. (2016) · Oncotarget · doi:10.18632/oncotarget.9366 · Cited by 32

ΔNp63α suppresses cells invasion by downregulating PKCγ/Rac1 signaling through miR-320a

Aljagthmi, A. A., Hill, N. T., Cooke, M., Kazanietz, M. G., Abba, M. C., Long, W., & Kadakia, M. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1921-6 · Cited by 31

The microRNA feedback regulation of p63 in cancer progression

Lin, C., Li, X., Zhang, Y., Guo, Y., Zhou, J., Gao, K., Dai, J., Hu, G. M., Lv, L., Du, J., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.3020 · Cited by 31

Interplay between ΔNp63 and miR-138-5p regulates growth, metastasis and stemness of oral squamous cell carcinoma

Zhuang, Z., Xie, N., Hu, J. R., Yu, P., Wang, C., Hu, X., Han, X., Hou, J., Huang, H., & Liu, X. (2017) · Oncotarget · doi:10.18632/oncotarget.15752 · Cited by 31

Differential expression and androgen regulation of microRNAs and metalloprotease 13 in breast cancer cells

Ahram, M. A., Mustafa, E. H., Zaza, R., Hammad, S. A., Alhudhud, M., Bawadi, R., & Zihlif, M. A. (2017) · Cell Biology International · doi:10.1002/cbin.10841 · Cited by 31

Spatiotemporal Regulation of ΔNp63 by TGFβ-Regulated miRNAs Is Essential for Cancer Metastasis

Bui, N. H. B., Napoli, M., Davis, A. J., Abbas, H. A., Rajapakshe, K., Coarfa, C., & Flores, E. R. (2020) · Cancer Research · doi:10.1158/0008-5472.can-19-2733 · Cited by 31

The role of microRNAs in prostate cancer progression.

Lo, U., Yang, D., & Hsieh, J. (2013) · PubMed Central · doi:10.3978/j.issn.2223-4683.2013.08.01 · Cited by 31

Arf tumor suppressor and miR-205 regulate cell adhesion and formation of extraembryonic endoderm from pluripotent stem cells

Li, C., Finkelstein, D., & Sherr, C. J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302184110 · Cited by 32

Tumor Protein p63/microRNA Network in Epithelial Cancer Cells

Ratovitski, E. A. (2013) · Current Genomics · doi:10.2174/13892029113146660011 · Cited by 30

MicroRNA‐205 inhibits cancer cell migration and invasion via modulation of centromere protein F regulating pathways in prostate cancer

Nishikawa, R., Goto, Y., Kurozumi, A., Matsushita, R., Enokida, H., Kojima, S., Naya, Y., Nakagawa, M., Ichikawa, T., & Seki, N. (2015) · International Journal of Urology · doi:10.1111/iju.12829 · Cited by 29

p63 Isoforms Regulate Metabolism of Cancer Stem Cells

D’Aguanno, S., Barcaroli, D., Rossi, C., Zucchelli, M., Ciavardelli, D., Cortese, C., Cola, A. D., Volpe, S., D’Agostino, D., Todaro, M., et al. (2014) · Journal of Proteome Research · doi:10.1021/pr4012574 · Cited by 29

The Genomic Landscape of Prostate Cancer

Spans, L., Clinckemalie, L., Helsen, C., Vanderschueren, D., Boonen, S., Lerut, E., Joniau, S., & Claessens, F. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140610822 · Cited by 32

P63 regulates tubular formation via epithelial-to-mesenchymal transition

Zhang, Y., Yan, W., & Chen, X. (2013) · Oncogene · doi:10.1038/onc.2013.101 · Cited by 29

Unraveling cancer lineage drivers in squamous cell carcinomas

Guan, Y., Wang, G., Fails, D. M., Nagarajan, P., & Ge, Y. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2019.107448 · Cited by 30

MicroRNA-155 and cancer metastasis: Regulation of invasion, migration, and epithelial-to-mesenchymal transition

Moutabian, H., Radi, U. K., Saleman, A. Y., Adil, M., Zabibah, R. S., Chaitanya, M., Saadh, M. J., Jawad, M. J., Hazrati, E., Bagheri, H., et al. (2023) · Pathology - Research and Practice · doi:10.1016/j.prp.2023.154789 · Cited by 30

The strong propensity of Cadherin‐23 for aggregation inhibits cell migration

Sannigrahi, M. K., Srinivas, C. S., Deokate, N., & Rakshit, S. (2019) · Molecular Oncology · doi:10.1002/1878-0261.12469 · Cited by 27

The Impact of Mutant p53 in the Non-Coding RNA World

Agostino, S. D. (2020) · Biomolecules · doi:10.3390/biom10030472 · Cited by 28

miR-429 inhibits glioma invasion through BMK1 suppression

Chen, W., Zhang, B., Guo, W.-J., Gao, L., Shi, L., Li, H., Lu, S., Liu, Y., & Li, X. (2015) · Journal of Neuro-Oncology · doi:10.1007/s11060-015-1887-x · Cited by 28

p53 overexpression is a prognosticator of poor outcome in esophageal cancer

Melling, N., Norrenbrock, S., Kluth, M., Simon, R., Hube‐Magg, C., Steurer, S. A., Hinsch, A., Burandt, E., Jacobsen, F., Wilczak, W., et al. (2019) · Oncology Letters · doi:10.3892/ol.2019.10020 · Cited by 27

Coix Seed Oil Exerts an Anti–Triple-Negative Breast Cancer Effect by Disrupting miR-205/S1PR1 Axis

Fang, T., Jiang, Y., Chen, L., Huang, L., Tian, X.-H., Zhou, Y., Nagle, D. G., & Zhang, D. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.529962 · Cited by 28

Dextran-Curcumin Nanosystems Inhibit Cell Growth and Migration Regulating the Epithelial to Mesenchymal Transition in Prostate Cancer Cells

Bevacqua, E., Curcio, M., Saletta, F., Vittorio, O., Cirillo, G., & Tucci, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137013 · Cited by 26

LncRNA MIR205HG accelerates cell proliferation, migration and invasion in hepatoblastoma through the activation of MAPK signaling pathway and PI3K/AKT signaling pathway

Zhang, W., Feng, L., Li, Q., Sun, H., Li, F., Jiao, Z., & Lei, J. (2022) · Biology Direct · doi:10.1186/s13062-021-00309-3 · Cited by 26

Role of MicroRNAs in Treatment Response in Prostate Cancer

Razdan, A., SOUZA, P. D., & Roberts, T. L. (2018) · Current Cancer Drug Targets · doi:10.2174/1568009618666180315160125 · Cited by 27

The functions of ocu-miR-205 in regulating hair follicle development in Rex rabbits

Liu, G., Li, S., Liu, H., Zhu, Y., Bai, L., Sun, H., Gao, S., Jiang, W., & Li, F. (2020) · BMC Developmental Biology · doi:10.1186/s12861-020-00213-5 · Cited by 27

ΔNp63 Expression is a Protective Factor of Progression in Clinical High Grade T1 Bladder Cancer

Gaya, J. M., López-Martínez, J. M., Karni-Schmidt, O., Bonal, D. M., Ferran Algaba, B., Palou, J., Villavicencio, H., Benson, M. C., Cordon‐Cardo, C., & Castillo-Martín, M. (2014) · The Journal of Urology · doi:10.1016/j.juro.2014.10.098 · Cited by 25

ΔNp63α and microRNAs: leveraging the epithelial-mesenchymal transition

Stacy, A. J., Craig, M. P., Sakaram, S., & Kadakia, M. (2016) · Oncotarget · doi:10.18632/oncotarget.13797 · Cited by 26

miR-26a induced the suppression of tumor growth of cholangiocarcinoma via KRT19 approach

Wang, P., & Lv, L. (2016) · Oncotarget · doi:10.18632/oncotarget.13229 · Cited by 24

ΔNp63α in cancer: importance and therapeutic opportunities

Fisher, M. L., Balinth, S., & Mills, A. A. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.08.003 · Cited by 26

The miR-124-p63 feedback loop modulates colorectal cancer growth

Liu, K., Yao, H., Lei, S., Xiong, L., Qi, H., Qian, K., Liu, J., Wang, P., & Zhao, H. (2017) · Oncotarget · doi:10.18632/oncotarget.16248 · Cited by 24

Tumor‐suppressive roles of ΔNp63β‐miR‐205 axis in epithelial–mesenchymal transition of oral squamous cell carcinoma via targeting ZEB1 and ZEB2

Hashiguchi, Y., Kawano, S., Goto, Y., Yasuda, K., Kaneko, N., Sakamoto, T., Matsubara, R., Jinno, T., Maruse, Y., Tanaka, H., et al. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.26267 · Cited by 24

Epigenetic Regulation of iASPP-p63 Feedback Loop in Cutaneous Squamous Cell Carcinoma

Robinson, D. J., Patel, A. A., Purdie, K. J., Wang, J., Rizvi, H., Hufbauer, M., Ostano, P., Akgũl, B., Chiorino, G., Harwood, C. A., et al. (2019) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2019.01.020 · Cited by 24

Correction of Mutant p63 in EEC Syndrome Using siRNA Mediated Allele-Specific Silencing Restores Defective Stem Cell Function

Barbaro, V., Nasti, A. A., Vecchio, C. D., Ferrari, S., Migliorati, A., Raffa, P., Lariccia, V., Nespeca, P., Biasolo, M. A., Willoughby, C. E., et al. (2016) · Stem Cells · doi:10.1002/stem.2343 · Cited by 24

p63 transcriptionally regulates the expression of matrix metallopeptidase 13

Celardo, I., Antonov, A., Amelio, I., Annicchiarico‐Petruzzelli, M., & Melino, G. (2014) · Oncotarget · doi:10.18632/oncotarget.1778 · Cited by 25

Human papillomavirus E7 induces p63 expression to modulate DNA damage response

Eldakhakhny, S., Zhou, Q., Crosbie, E. J., & Sayan, B. S. (2018) · Cell Death and Disease · doi:10.1038/s41419-017-0149-6 · Cited by 23

ΔNp63α expression induces loss of cell adhesion in triple-negative breast cancer cells

Nekulová, M., Holčáková, J., Gu, X., Hrabal, V., Galtsidis, S., Orzol, P., Liu, Y., Logotheti, S., Zoumpourlis, V., Nylander, K., et al. (2016) · BMC Cancer · doi:10.1186/s12885-016-2808-x · Cited by 21

Oncogenic YAP mediates changes in chromatin accessibility and activity that drive cell cycle gene expression and cell migration

Fetiva, M. C., Liss, F., Gertzmann, D., Thomas, J., Gantert, B., Vogl, M., Sira, N., Weinstock, G., Kneitz, S., Ade, C. P., et al. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad107 · Cited by 22

Androgens downregulate miR-21 expression in breast cancer cells underlining the protective role of androgen receptor

Casaburi, I., Cesario, M. G., Donà, A., Rizza, P., Aquila, S., Avena, P., Lanzino, M., PELLEGRINO, M. A., Vivacqua, A., Tucci, P., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.7207 · Cited by 24

Metabolic pathways regulated by TAp73 in response to oxidative stress

Agostini, M., Annicchiarico‐Petruzzelli, M., Melino, G., & Rufini, A. (2016) · Oncotarget · doi:10.18632/oncotarget.8935 · Cited by 22

TRIM29 regulates the p63-mediated pathway in cervical cancer cells

Masuda, Y., Takahashi, H., & Hatakeyama, S. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.05.035 · Cited by 22

Metabolic profiling of human CD4+ cells following treatment with methotrexate and anti-TNF-α infliximab

Chimenti, M. S., Tucci, P., Candi, E., Perricone, R., Melino, G., & Willis, A. E. (2013) · Cell Cycle · doi:10.4161/cc.26067 · Cited by 21

The Potential of MicroRNAs as Non-Invasive Prostate Cancer Biomarkers: A Systematic Literature Review Based on a Machine Learning Approach

Bevacqua, E., Ammirato, S., Cione, E., Curcio, R., Dolce, V., & Tucci, P. (2022) · Cancers · doi:10.3390/cancers14215418 · Cited by 21

microRNA-205 in prostate cancer: Overview to clinical translation

Chauhan, N., Manojkumar, A., Jaggi, M., Chauhan, S. C., & Yallapu, M. M. (2022) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2022.188809 · Cited by 22

ΔNP63α Transcriptionally Activates Chemokine Receptor 4 (CXCR4) Expression to Regulate Breast Cancer Stem Cell Activity and Chemotaxis

DeCastro, A., Cherukuri, P., Balboni, A., & DiRenzo, J. (2014) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-14-0194 · Cited by 20

How MicroRNAs Command the Battle against Cancer

Wu, H. H., Leng, S., Sergi, C. M., & Leng, R. P. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25115865 · Cited by 22

Negative feedback between TAp63 and Mir-133b mediates colorectal cancer suppression

Dai, J., Wu, H., Zhang, Y., Gao, K., Hu, G. M., Guo, Y., Lin, C., & Li, X. (2016) · Oncotarget · doi:10.18632/oncotarget.13515 · Cited by 18

The ambiguous role of microRNA-205 and its clinical potential in pancreatic ductal adenocarcinoma

Träger, M. M., Rehkämper, J., Ullerich, H., Steinestel, K., Wardelmann, E., Senninger, N. J., & Dhayat, S. A. (2018) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-018-2755-9 · Cited by 19

Long non‑coding RNAs in prostate tumorigenesis and therapy (Review)

Jiang, G., SU, Z., Liang, X., Huang, Y., Lan, Z., & Jiang, X. (2020) · Molecular and Clinical Oncology · doi:10.3892/mco.2020.2146 · Cited by 19

Network biology approach to epithelial–mesenchymal transition in cancer metastasis: three stage theory

Tanaka, H., & Ogishima, S. (2015) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjv035 · Cited by 19

Nanoparticle‐based targeted cancer strategies for non‐invasive prostate cancer intervention

Farina, N. H., Zingiryan, A., Vrolijk, M. A., Perrapato, S. D., Ades, S., Stein, G. S., Lian, J. B., & Landry, C. C. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26593 · Cited by 18

Pir2/Rnf144b is a potential endometrial cancer biomarker that promotes cell proliferation

Zhou, Q., Eldakhakhny, S., Conforti, F., Crosbie, E. J., Melino, G., & Sayan, B. S. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0521-1 · Cited by 18

MicroRNA‑205‑5p regulates extracellular matrix production in hyperplastic scars by targeting Smad2

Qi, J., Liu, Y., Hu, K., Zhang, Y., Wu, Y., & Zhang, X. (2019) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2019.7187 · Cited by 18

The p53 Family Members p63 and p73 Roles in the Metastatic Dissemination: Interactions with microRNAs and TGFβ Pathway

Calleja, L. R., Lavaud, M., Tesfaye, R. A., Royer, B. B.-L., Baud’huin, M., Georges, S., Lamoureux, F., Verrecchia, F., & Ory, B. (2022) · Cancers · doi:10.3390/cancers14235948 · Cited by 18

The tumour suppressor DiRas3 interacts with C‐RAF and downregulates MEK activity to restrict cell migration

Klingauf, M., Beck, M., Berge, U., Turgay, Y., Heinzer, S., Horváth, P., & Kroschewski, R. (2012) · Biology of the Cell · doi:10.1111/boc.201200030 · Cited by 18

Targeted Knockdown of the Kinetochore Protein D40/Knl-1 Inhibits Human Cancer in a p53 Status-Independent Manner

Urata, Y. N., Takeshita, F., Tanaka, H., Ochiya, T., & Takimoto, M. (2015) · Scientific Reports · doi:10.1038/srep13676 · Cited by 20

ΔNp63α attenuates tumor aggressiveness by suppressing miR-205/ZEB1-mediated epithelial–mesenchymal transition in cervical squamous cell carcinoma

Zhao, W., Wang, H., Han, X., Ma, J., Zhou, Y., Chen, Z., Zhou, H., Xu, H., Sun, Z., Kong, B., et al. (2016) · Tumor Biology · doi:10.1007/s13277-016-4921-5 · Cited by 18

ΔNp63α promotes adhesion of metastatic prostate cancer cells to the bone through regulation of CD82

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The p53 Family in Brain Disease

Agostini, M., Melino, G., & Bernassola, F. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7302 · Cited by 19

MicroRNAs that affect prostate cancer: emphasis on prostate cancer in African Americans

Jones, J., Grizzle, W. E., Wang, H., & Yates, C. C. (2013) · Biotechnic & Histochemistry · doi:10.3109/10520295.2013.807069 · Cited by 17

High miR-205 expression in normal epithelium is associated with biochemical failure - an argument for epithelial crosstalk in prostate cancer?

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The role of oncogenic Ras in human skin tumorigenesis depends on the clonogenic potential of the founding keratinocytes

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Overexpression of oxidored-nitro domain containing protein 1 induces growth inhibition and apoptosis in human prostate cancer PC3 cells

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Unnatural killer cells to prevent bloodborne metastasis: inspiration from biology and engineering

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p53 Mutation in the Genesis of Metastasis

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The “Sharp”blade against HIF-mediated metastasis

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TAp63 regulates oncogenic miR-155 to mediate migration and tumour growth

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IR-Surviving NSCLC Cells Exhibit Different Patterns of Molecular and Cellular Reactions Relating to the Multifraction Irradiation Regimen and p53-Family Proteins Expression

Alhaddad, L., Pustovalova, M. V., Blokhina, T., Chuprov‐Netochin, R. N., Osipov, A. N., & Leonov, S. V. (2021) · Cancers · doi:10.3390/cancers13112669 · Cited by 15

miRNAs as drivers of TMPRSS2-ERG negative prostate tumors in African American men

Campbell, M. J. (2016) · Frontiers in bioscience · doi:10.2741/4482 · Cited by 14

MicroRNA-133b is regulated by TAp63 while no gene mutation is present in colorectal cancer

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Role of exosomal small RNA in prostate cancer metastasis

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TAp63 and ΔNp63 (p40) in prostate adenocarcinomas: ΔNp63 associates with a basal-like cancer stem cell population but not with metastasis

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In-Silico Integration Approach to Identify a Key miRNA Regulating a Gene Network in Aggressive Prostate Cancer

Cava, C., Bertoli, G. R., Colaprico, A., Bontempi, G., Mauri, G., & Castiglioni, I. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19030910 · Cited by 13

Nectin‐4 and p63 immunohistochemical expression in canine prostate tumourigenesis

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ERK3 is transcriptionally upregulated by ∆Np63α and mediates the role of ∆Np63α in suppressing cell migration in non-melanoma skin cancers

Alshammari, E. S., Aljagthmi, A. A., Stacy, A. J., Bottomley, M., Shamma, H. N., Kadakia, M., & Long, W. (2021) · BMC Cancer · doi:10.1186/s12885-021-07866-w · Cited by 13

Convergence of dispersed regulatory mutations predicts driver genes in prostate cancerPreprint

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Murine double minute 2, a potential p53-independent regulator of liver cancer metastasis

Ranjan, A., Bera, K., & Iwakuma, T. (2016) · Hepatoma Research · doi:10.20517/2394-5079.2015.67 · Cited by 12

Loss of p63 and its miR-205 target results in enhanced cell migration and metastasis in prostate cancer

Tucci, P. (2012) · Archive of Doctoral Theses and Digital Collections (University of Calabria)

miR-573 inhibits prostate cancer metastasis by regulating epithelial-mesenchymal transition

Wang, L., Song, G., Tan, W., Qi, M., Zhang, L., Chan, J., Yu, J., Han, J., & Han, B. (2015) · Oncotarget · doi:10.18632/oncotarget.5427 · Cited by 65

miR-135b inhibits tumour metastasis in prostate cancer by targeting STAT6

Wang, N., Tao, L., ZHONG, H., Zhao, S., Yu, Y., Yu, B., Chen, X., Gao, J., & WANG, R. (2015) · Oncology Letters · doi:10.3892/ol.2015.3970 · Cited by 42

Regulatory Role of mir-203 in Prostate Cancer Progression and Metastasis

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MiR-203 controls proliferation, migration and invasive potential of prostate cancer cell lines

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