Pleckstrin homology-like domain, family A, member 1 (PHLDA1) and cancer
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Citações na Scopus
50
Tipo de produção
article
Data de publicação
2016
Título da Revista
ISSN da Revista
Título do Volume
Editora
SPANDIDOS PUBL LTD
Autores
Citação
BIOMEDICAL REPORTS, v.4, n.3, p.275-281, 2016
Resumo
Pleckstrin homology-like domain, family A, member 1 (PHLDA1) encodes a member of an evolutionarily conserved pleckstrin homology-related domain protein family. It was first identified as a potential transcription factor required for Fas expression and activation-induced apoptosis in mouse T cell hybridomas. The exact molecular and biological functions of PHLDA1 remain to be elucidated. However, its expression is induced by a variety of external stimuli and there is evidence that it may function as a transcriptional activator that acts as a mediator of apoptosis, proliferation, differentiation and cell migration dependent on the cellular type and context. Recently, PHLDA1 has received attention due to its association with cancer. In the present review, the current knowledge of PHLDA1 protein structure, expression regulation and function is summarized. In addition, the current data in the literature is reviewed with regards to the role of PHLDA1 in cancer pathogenesis.
Palavras-chave
PHLDA1, pleckstrin homology-like, cancer, tumor suppressor gene, oncogene, downregulation, stem cell
Referências
- Frank D, 1999, MAMM GENOME, V10, P1150, DOI 10.1007/s003359901182
- Gomes I, 1999, J NEUROCHEM, V73, P612, DOI 10.1046/j.1471-4159.1999.0730612.x
- Hanahan D, 2011, CELL, V144, P646, DOI 10.1016/j.cell.2011.02.013
- Hinz T, 2001, CELL SIGNAL, V13, P345, DOI 10.1016/S0898-6568(01)00141-3
- Butland SL, 2007, BMC GENOMICS, V8, DOI 10.1186/1471-2164-8-126
- Carlisle RE, 2012, AM J PHYSIOL-RENAL, V303, pF467, DOI 10.1152/ajprenal.00481.2011
- Lemmon MA, 2000, BIOCHEM J, V350, P1, DOI 10.1042/0264-6021:3500001
- Coutinho-Camillo CM, 2013, VIRCHOWS ARCH, V463, P31, DOI 10.1007/s00428-013-1438-9
- Ohyama M, 2006, J CLIN INVEST, V116, P249, DOI 10.1172/JCI26043
- Wu SF, 2010, J CLIN ENDOCR METAB, V95, P1220, DOI 10.1210/jc.2009-1662
- Liu F, 2011, MOL REPROD DEV, V78, P283, DOI 10.1002/mrd.21304
- WILLIAMSON MP, 1994, BIOCHEM J, V297, P249
- Sellheyer K, 2011, BRIT J DERMATOL, V164, P141, DOI 10.1111/j.1365-2133.2010.10045.x
- Oberg HH, 2004, CELL DEATH DIFFER, V11, P674, DOI 10.1038/sj.cdd.4401407
- Moad AIH, 2013, CELL BIOCHEM BIOPHYS, V66, P567, DOI 10.1007/s12013-012-9504-5
- Kuske MDA, 2000, CYTOGENET CELL GENET, V89, P1, DOI 10.1159/000015575
- Wang RX, 1998, J IMMUNOL, V161, P2201
- Nagai MA, 2007, BREAST CANCER RES TR, V106, P49, DOI 10.1007/s10549-006-9475-6
- Shang YL, 2013, CURR CANCER DRUG TAR, V13, P915
- Rho J, 2001, MOL CELL BIOL, V21, P8365, DOI 10.1128/MCB.21.24.8365-8370.2001
- Pasquier J, 2015, J ONCOL, DOI 10.1155/2015/792182
- Hossain GS, 2003, J BIOL CHEM, V278, P30317, DOI 10.1074/jbc.M212897200
- Lemmon MA, 2002, FEBS LETT, V513, P71, DOI 10.1016/S0014-5793(01)03243-4
- Guezguez A, 2014, EXP CELL RES, V322, P355, DOI 10.1016/j.yexcr.2014.02.009
- Kastrati I, 2015, ONCOGENE, V34, P2309, DOI 10.1038/onc.2014.180
- Scheffzek K, 2012, FEBS LETT, V586, P2662, DOI 10.1016/j.febslet.2012.06.006
- Sohn EJ, 2010, CANCER RES, V70, P1154, DOI 10.1158/0008-5472.CAN-09-1993
- Neef R, 2002, CANCER RES, V62, P5920
- Xu Q, 2010, J MOL BIOL, V396, P31, DOI 10.1016/j.jmb.2009.11.006
- Joo JH, 2007, CANCER RES, V67, P7929, DOI 10.1158/0008-5472.CAN-07-0931
- Ren L, 2015, ONCOTARGET, V6, P29469, DOI 10.18632/oncotarget.5177
- Murohashi M, 2010, BRIT J CANCER, V102, P206, DOI 10.1038/sj.bjc.6605468
- Mohammad RM, 2015, SEMIN CANCER BIOL, V35, pS78, DOI 10.1016/j.semcancer.2015.03.001
- Zhao P, 2015, INT J CLIN EXP PATHO, V8, P5230
- Park CG, 1996, IMMUNITY, V4, P583, DOI 10.1016/S1074-7613(00)80484-7
- Johnson EO, 2011, J CELL SCI, V124, P2711, DOI 10.1242/jcs.084970
- Chiu ST, 2005, CANCER EPIDEM BIOMAR, V14, P437, DOI 10.1158/1055-9965.EPI-04-0396
- Marchiori AC, 2008, BRAZ J MED BIOL RES, V41, P579, DOI 10.1590/S0100-879X2008005000029
- Boro A, 2012, INT J CANCER, V131, P2153, DOI 10.1002/ijc.27472
- Hayashida N, 2006, EMBO J, V25, P4773, DOI 10.1038/sj.emboj.7601370
- Toyoshima Y, 2004, J BIOL CHEM, V279, P25898, DOI 10.1074/jbc.M400661200
- Liu CR, 2015, J NEUROGENET, V29, P41, DOI 10.3109/01677063.2015.1073275
- Li GY, 2014, PLOS ONE, V9, DOI 10.1371/journal.pone.0106349
- Murata T, 2014, EXP CELL RES, V320, P247, DOI 10.1016/j.yexcr.2013.10.023
- Oberst MD, 2008, BMC CANCER, V8, DOI 10.1186/1471-2407-8-189
- Sakthianandeswaren A, 2011, CANCER RES, V71, P3709, DOI 10.1158/0008-5472.CAN-10-2342