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The role of tumor protein 53 mutations in common human cancers and targeting the murine double minute 2-p53 interaction for cancer therapy.
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PMID:  23115424     Owner:  NLM     Status:  PubMed-not-MEDLINE    
The gene TP53 (also known as protein 53 or tumor protein 53), encoding transcription factor P53, is mutated or deleted in half of human cancers, demonstrating the crucial role of P53 in tumor suppression. There are reports of nearly 250 independent germ line TP53 mutations in over 100 publications. The P53 protein has the structure of a transcription factor and, is made up of several domains. The main function of P53 is to organize cell defense against cancerous transformation. P53 is a potent transcription factor that is activated in response to diverse stresses, leading to the induction of cell cycle arrest, apoptosis or senescence. The P53 tumor suppressor is negatively regulated in cells by the murine double minute 2 (MDM2) protein. Murine double minute 2 favors its nuclear export, and stimulates its degradation. Inhibitors of the P53-MDM2 interaction might be attractive new anticancer agents that could be used to activate wild-type P53 in tumors. Down regulation of MDM2 using an small interfering RNA (siRNA) approach has recently provided evidence for a new role of MDM2 in the P53 response, by modulating the inhibition of the cyclindependent kinase 2 (cdk2) by P21/WAF1 (also known as cyclin-dependent kinase inhibitor 1 or CDK-interacting protein 1).
Tayebeh Hamzehloie; Majid Mojarrad; Mohammad Hasanzadeh Nazarabadi; Sahar Shekouhi
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Iranian journal of medical sciences     Volume:  37     ISSN:  1735-3688     ISO Abbreviation:  Iran J Med Sci     Publication Date:  2012 Mar 
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Created Date:  2012-11-01     Completed Date:  2012-11-02     Revised Date:  2013-05-30    
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Nlm Unique ID:  8104374     Medline TA:  Iran J Med Sci     Country:  Iran    
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Languages:  eng     Pagination:  3-8     Citation Subset:  -    
Department of Medical Genetics, Mashhad University of Medical Sciences, Mashhad, Iran.
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Journal ID (nlm-ta): Iran J Med Sci
Journal ID (iso-abbrev): Iran J Med Sci
Journal ID (publisher-id): IJMS
ISSN: 0253-0716
ISSN: 1735-3688
Publisher: Shiraz University of Medical Sciences, Shiraz, Iran
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© 2012: Iranian Journal of Medical Sciences
Received Day: 11 Month: 7 Year: 2011
Revision Received Day: 8 Month: 10 Year: 2011
Accepted Day: 13 Month: 11 Year: 2011
Print publication date: Month: 3 Year: 2012
Volume: 37 Issue: 1
First Page: 3 Last Page: 8
PubMed Id: 23115424
ID: 3470295
Publisher Id: IJMS-37-03

The Role of Tumor Protein 53 Mutations in Common Human Cancers and Targeting the Murine Double Minute 2–P53 Interaction for Cancer Therapy
Tayebeh Hamzehloie
Majid Mojarrad
Mohammad Hasanzadeh_Nazarabadi
Sahar Shekouhi
Department of Medical Genetics, Mashhad University of Medical Sciences, Mashhad, Iran.
Correspondence: Correspondence: Mohammad Hasanzadeh_Nazarabadi PhD, Department of Medical Genetics, Mashhad University of Medical Sciences, Azadi Square, Mashhad, Iran. Tel: +98 511 8002246 Fax: +98 511 8002247 Email:


Tumor protein 52 (TP53) gene, which encodes transcription factor P53, maps to chromosome 17pl 3.1, spanning around 20 kilobase (kb) pairs, and comprises 11 exons.1 The P53 gene is well-suited to mutational spectrum analysis for several reasons. Since P53 mutations are common in many human cancers,2 its modest size (11 exons, 393 amino acids) permits study of the entire coding region. It is highly conserved in vertebrates, allowing extrapolation of data from animal models.3

Structural Features

The human P53 protein contains 393 amino acids, and has been divided structurally and functionally into four domains. The first 42 amino acids at the N-terminus constitute a transcriptional

activation domain that interacts with the basal transcriptional machinery in positively regulating gene expression. Amino acids 13–23 in the P53 protein are identical in a number of diverse species. The sequence-specific DNA-binding domain of P53 is localized between amino acid residues 102 and 292. This domain folds into a four-stranded and five-stranded antiparallel β sheet that in turn is a scaffold for two α-helical loops that interact directly with the DNA. Amino acid residues 324–355 are required for this oligomerization of the protein. The C-terminal 26 amino acids form an open protease sensitive domain composed of nine basic amino acid residues that bind to DNA and RNA readily with some sequence or structural preferences.4,5 Two promoters have been identified in the P53 gene. The first is located 100 to 250 bp upstream of the noncoding first exon, and the second, a stronger promoter, is located within the first intron.6 The TP53 gene contains 11 exons. It has two transcriptional start sites in exon 1, and alternative splicing occurs in intron 2 and between exons 9 and 10. The gene also contains an internal promoter and transcription initiation site in intron 4.7 Sequence comparison of the P53 protein from different species shows five highly conserved regions. Two common polymorphic variants of P53 exist, arising from a single base-pair substitution at codon 72, encoding either a proline or an arginine residue.8,9 Although both polymorphic forms share similar growth-suppressive activities, recent studies suggesting subtle differences in their regulation and potency may be reflected in increased cancer susceptibility in some individuals.10,11 Presence of single nucleotide polymorphism (SNP) in the MDM2 promoter has been associated with earlier tumor genesis in patients with Li–Fraumeni syndrome, as well as decreased survival in patients with chronic lymphocytic leukemia (CLL). In addition, cells homozygous [G/G] for SNP 309 were found to have 10-fold increased resistance to topoisomerase II inhibiting drugs.12 The p73 gene has been mapped to chromosome 1p36.3, a locus that is deleted in neuroblastoma and some other human cancers. The P73 gene encodes at least four distinct isoforms; the full-length version, which gives rise to the protein called P73α, and three splice variants, which encode proteins referred to as P73β, γ and δ. P73 has been shown to mediate at least some functions in common with P53, including apoptosis, transcriptional transactivation of P21WAF1/CIP1, a known target of P53, and suppression of cell growth. But unfortunately, a contribution of P63 to tumor suppression has not yet been established.13


Wild-type TP53 functions in checkpoint control after DNA damage, resulting in either a delay in cell cycle progression at the G/S border to allow DNA repair or apoptosis. TP53 has also been implicated directly in DNA repair and in G2 arrest.14 Under normal conditions, P53 is a short-lived protein that is present in cells at a barely detectable level. Upon exposure of cells to various forms of exogenous stress, such as DNA damage, heat shock, hypoxia, and etc., there is a stabilization of P53, which is responsible for an ensuing cascade of events, resulting in either cell cycle arrest or in apoptosis.15 Further functions of P53 include senescence, and angiogenesis, centrosome duplication, adhesion and metastasis.16 A role for P53 in preventing malignant progression was subsequently demonstrated by the observations that transfection of P53 into cultured cells inhibited transformation by a number of oncogenes, and that mice lacking the P53 gene rapidly developed tumors with high incidence.14 Although mice deleted of the P53 gene show a high incidence of cancer, nevertheless their viability and relatively normal development indicated that P53 function is not essential for cell growth and differentiation.15


Apoptosis is a form of programmed cell death. Both the death-receptor-associated pathways and the Apaf-1-dependentapoptotic pathway (Apoptotic protease activating factor 1) have been shown to be involved in mediating P53-dependent cell death. Other potential apoptotic transcriptional targets of P53 include Insulin-like growth factor-binding protein 3 (IGFBP-3) and P53-activated gene (PAG608).13 The adenovirus EIA, Human papillomaviruses (HPV E7) and SV40 huge T proteins bind to Retinoblastoma Protein (PRb), and thereby inactivate PRb’s ability to restrain cell division.17 The human papilloma virus genome encodes the E6 oncogene product to bind to P53 and degrade it. Transgenic mice expressing E7 in the retina photoreceptor cells show extensive apoptosis. The expression of E7 in the same cells but in a P53-/-mouse results in a reduced frequency of apoptosis and an increased frequency of development of retinal tumors.5

Transcriptional Activation by P53

Accumulation of P53 in cells induces the P21 mediated inhibition of Cyclin D/cdk4 and cyclinE/cdk2, resulting in cell cycle arrest in G1.15 Many cellular genes have been shown to be transcriptional targets of P53.18 The growth arrest and DNA damage 45 (GADD45) gene is a member of a group of growth arrest and DNA damage-inducible genes (GADD), and is induced by ionizing radiation in many cell types containing wt P53.13 The gene PA26, another novel P53 target gene that belongs to the GADD family play a role in growth regulation.19 Another P53-target gene is IGFBP-3. Seven in absentia homolog (SIAH-1) has also been shown to play a role in P53-dependent cell-cycle arrest,20 ,21 and the 14-3-3δ protein has been shown to be a potent P53-mediated regulator of G2–M progression.22 Apoptotic cellular changes have been shown to involve a family of Cysteine proteases called Caspases (ICE/CED-3 proteases),23 which can be activated through two main pathways, one involving the activation of death receptors, such as Fas/APO1 and DR5 at the cell surface, and the other involving Cytochrome-c dependent activation of the adaptor protein, Apaf-1.24

Transcriptional Repression by P53

In addition to activating genes with P53-binding sites, P53 can also repress promoters that lack the P53-binding element. A number of genes, including Interleukin-6, Nuclear Factor-kB RELA (NF kB), Cyclin A, Proliferating Cell Nuclear Antigen (PCNA), and a number of metastasis-related genes,24 have been shown to be transcriptionally repressed by P53 in this way. Additionally, both RNA polymerase II and III transcription can be repressed by P53.25

Germline TP53 Mutations

Mutant P53 protein can also inhibit the normal function of wild type P53 protein. Approximately 50% of all human tumors carry a P53 mutation, and at least 52 different types of tumor have P53 mutations.26,27 Detection of P53 abnormalities may have diagnostic, prognostic, and therapeutic implications. Point mutations which alter P53 function are distributed over a large region of the molecule.1 At the molecular level, 53% of germ line P53 mutations are G:C to A:T transitions at CpG, which are naturally occurring sites of methylation in the genome.28 Recently mutations of the oligomerization domain have been isolated from an LFS and an LFL family affecting respectively codon 344 (Leu to Pro) and 337 (Arg to Cys). Point mutations in the oligomerization domain can disrupt P53 function.26 Although the mutations spread over essentially the entire gene, nevertheless there is considerable clustering of mutations within the central region of the protein. The majority of mutations are missense, with alterations at only five codons representing 25% of all known mutations (codons 175, 245, 248, 249 and 273).14 Mutations in codons 248, 273, 245, 175, and 282 are the most common in both sporadic tumors and the germline, although their ranking is somewhat different sporadic tumors and the germ line.27 In addition, Mutant P53 gene may have a role in the persistence of cancer cells and development of basal and squamous cell carcinomas.29

Mutations of CHK1 and CHK2 in LFS

Checkpoint kinase 2 (Chk2) is a DNA damage-activated protein kinase that lies downstream of ATM in this pathway. Heterozygous germ line mutations in Chk2 have been identified in a subset of patients with Li-Fraumeni syndrome, a highly penetrant familial cancer phenotype, suggesting that Chk2 is a tumor suppressor gene.27 These two are essential for prevention of neoplastic transformation. Several proteins involved in this pathway including P53, breast cancer type 2 suceptibility (BRCA1), and Ataxia telangiectasia mutated (ATM) are frequently mutated in human cancer. In a kindred with Li-Fraumeni syndrome (LFS) without an inherited TP53 mutation, previously has been reported a truncating mutation (1100delC) in Checkpoint kinase 2 (CHK2), encoding a kinase that phosphorylates P53 on Ser20. And also CHK2 missense mutation (R145W) has been reported in another LFS family. Both 1100delC and R145W germ-line mutations in CHK2 are associated with loss of the wild-type allele in the corresponding tumor specimens, and neither tumor harbors a somatic TP53 mutation.30 The cell cycle checkpoint kinases CHK1 and CHK2 act upstream of P53 in DNA damage responses. CHK2 is a human homologue of Cds1 in Schizosaccharomyces pombe and Rad53 in Saccharomyces cerevisiae, and CHK1 is a human homologue of the S. pombe checkpoint kinase Chk1.31

MDM2: A Master Regulator of P53 Stability and Activity

MDM2 was originally identified as an amplified gene on double minute chromosomes in spontaneously transformed 3T3 cells. MDM2 negatively regulates P53 stability and transcriptional function. Its human counterpart, the human homologue of murine (HDM2) encodes a 90-kDa (491 amino acids) nuclear phosphoprotein that is over expressed in several types of human tumors. The HDM2 gene spans f33 kb of genomic DNA and also consists of 12 exons.32 In normal cells, MDM2 and P53 regulate each other through an auto regulatory feedback.33 Murine double minute directly binds to residues within the N-terminal transactivation domain of P53, a P53 target and E3 ligase that promotes the degradation of P53 through the proteasome pathway.34 Following stress, stabilization of P53 activates numerous pathways triggering a cellular response that can lead to growth arrest, senescence, differentiation, or apoptosis.35,36 DNA-damage-induced phosphorylation of P53 promotes a further conformational change, which is catalyzed by the prolyl isomerase Pin1. This leads to detachment of MDM2 from P53 and to its consequent stabilization and increase of DNA-binding and transactivation activities.37-39 P53 mutants are unable to activate the expression of MDM2, and are therefore, usually stable and expressed at high levels. Down regulation of MDM2 using an SiRNA approach has recently provided evidence for a new role of MDM2 in the P53 response, by modulating the inhibition of the cyclindependent kinase 2 (cdk2) by P21.40

Regulation of P53 by MDM2

Murine double minute regulates P53 in three different ways. Murine double minute binds to the P53 transactivation domain and inhibits its transcriptional activity;27 exports P53 out of the nucleus, promoting its degradation and rendering it inaccessible to the target genes; and promotes proteasome-mediated degradation of P53 by functioning as an E3 ubiquitin ligase. Therefore, in the presence of MDM2, the P53 protein is inactivated and does not stimulate the expression of genes involved in apoptosis, cell cycle arrest, or DNA repair. In some tumors where MDM2 is over expressed, P53 is constantly inhibited and tumor growth is favored. The inactivation of MDM2 in these tumors should activate the P53 pathway and as a possible consequence should activate apoptosis.4

Strategies to Target MDM2 in Tumors

Antisense oligonucleotides should decrease the cellular levels of MDM2 (Strategy 1). Compounds that inhibit the ubiquitin ligase activity of MDM2 could prevent P53 degradation (Strategy 2). P14RF (an alternate reading frame product of the cyclin-dependent kinase inhibitor 2A (CDKN2A) locus) acts by blocking MDM2-dependent degradation and transcriptional silencing of P53. P14ARF mimics should therefore, activate the P53 pathway (Strategy 3). Inhibitors of the P53-MDM2 interaction should release P53 from MDM2 and as a consequence should activate P53 tumor suppressor activity (Strategy 4).4 The stability of the P53 protein in mammals is primarily regulated in non-transformed cells by the interplay of two proteins, HDM2 and P14Arf in humans.15 In addition to P53, MDM2 has been reported to promote the degradation of P21, MDMX, retinoblastoma protein (PRB), MTBP, Ecadherin, homeodomain-interacting protein kinase 2 (HIPK2), junction mediating and regulatory protein (IMY).

Targeting the MDM2-P53 Interaction for Cancer Therapy

Because the interaction between MDM2 and P53 is a primary mechanism for inhibition of the P53 function in cancers retaining wild-type P53, targeting the MDM2-P53 interaction by small molecules to reactivate P53 has emerged as a promising new cancer therapeutic strategy, small-molecule MDM2 inhibitors, known as Nutlins, was reported in 2004. The MDM2-P53 interaction is mediated by a well-defined hydrophobic surface pocket in MDM2 and four key hydrophobic residues in P53, namely Phe19, Leu22, Trp23, and Leu26. This well-defined interaction has provided the basis for the design of nonpeptide, drug-like small-molecule inhibitors of the MDM2-P53 interaction to reactivate P53. Restoration of P53 by a genetic approach in the absence of MDM2 results in severe pathologic damage to radiosensitive mouse tissues and the death of all animals within five days.16 In contrast, both Nutlin-3,34 and MI-219,4 show little toxicity to animals at therapeutically efficacious dose-schedules.16 Furthermore, a whole range of small drugs is available, which act on different aspects of mutant P53 activities. These drugs are now ready to move into clinical trials, either alone or in combination with classical therapeutic approaches. In the next 10 years, such molecules are expected to contribute in an important way to the large panel of specific drugs that will be required to deliver the promises of evidence-based and personalized medicine.41,42

Link between P53 and MicroRNA

MicroRNAs, which silence the expression of target genes through the RNA interference pathway, are commonly down regulated in human cancers.43 MicroRNAs have emerged as key post-transcriptional regulators of gene expression, involved in diverse physiological and pathological processes. Although miRNAs can function as both tumor suppressors and oncogenes in tumor development, a widespread down regulation of miRNAs is commonly observed in human cancers. P53 enhances the post-transcriptional maturation of several miRNAs with growth-suppressive function, including microRNA 16-1(miR-1), miR-143 and miR-145 in response to DNA damage.44 Expression of miR-34 induces cell cycle arrest, and thereby acts together with other effectors of the P53 tumor suppressor network to inhibit inappropriate cell proliferation. Another group independently demonstrated that miR-34 is upregulated by P53 upon DNA damage and promotes apoptosis.45,46


Although P53 is not a typical cancer-specific antigen, its main role in the control of cell growth and apoptosis and frequent mutations in tumors make P53 a unique target for cancer therapy. Activation of the P53 tumor suppressor pathway in malignant tumors has been considered an attractive approach to cancer therapy, but its clinical potential is still unknown. The first potent and selective inhibitors of the P53–MDM2 interaction, the Nutlins, have been identified. Future studies of MDM2 inhibitors in the clinical setting are necessary to address their utility and possible advantages over the current standard therapy.

Conflict of Interest: None declared

1. Greenblatt MS,Bennett WP,Hollstein M,Harris CC. Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesisCancer ResYear: 1994544855788069852
2. Hollstein M,Rice K,Greenblatt MS,et al. Database of p53 gene somatic mutations in human tumors and cell linesNucleic Acids ResYear: 199422355157937055
3. Soussi T,May P. Structural aspects of the p53 protein in relation to gene evolutionOncogeneYear: 19905945522142762
4. Chène P. Inhibition of the p53-MDM2 interaction: targeting a protein-protein interfaceMol Cancer ResYear: 2004220814757842
5. Levine AJ. p53, the cellular gatekeeper for growth and divisionCellYear: 199788323319039259
6. Reisman D,Greenberg M,Rotter V. Human p53 oncogene contains one promoter upstream of exon 1 and a second, stronger promoter within intron 1Proc Natl Acad Sci USAYear: 1988855146502839831
7. Bourdon JC,Fernandes K,Murray-Zmijewski F,et al. p53 isoforms can regulate p53 transcriptional activityGenes DevYear: 20051921223716131611
8. Nikbakht Dastjerdi M. Analysis of TP53 Codon 72 Polymorphism in Mucinous and Non-Mucinous Colorectal Adenocarcinoma in Isfahan, IranIran J Med SciYear: 201035339
9. Nobori T,Miura K,Wu DJ,et al. Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancersNatureYear: 199436875368152487
10. Gonzalez-Zulueta M,Shibata A,et al. p16 gene in uncultured tumoursNatureYear: 199437018348028660
11. Sidransky D. Role of the p16 tumor suppressor gene in cancerJ Clin OncolYear: 19981611972069508208
12. Phillips CL,Gerbing R,Alonzo T,et al. MDM2 polymorphism increases susceptibility to childhood acute myeloid leukemia: a report from the Children's Oncology GroupPediatr Blood CancerYear: 2010552485320582981
13. Fisher D. Tumor suppressor genes in human cancerYear: 2001BostonHarvard Medical School
14. Varley JM,Evans DG,Birch JM. Li-Fraumeni syndrome-a molecular and clinical reviewBr J CancerYear: 1997761149218725
15. Boisvert FM,Lamond AI. p53-Dependent subcellular proteome localization following DNA damageProteomicsYear: 20101040879721080495
16. Shangary S,Wang S. Targeting the MDM2-p53 interaction for cancer therapyClin Cancer ResYear: 20081453182418765522
17. Beijersbergen RL,Bernards R. Cell cycle regulation by the retinoblastoma family of growth inhibitory proteinsBiochimica et biophysica acta. Biochim Biophys ActaYear: 1996128710320
18. Ko LJ,Prives C. p53: puzzle and paradigmGenes DevYear: 1996101054728654922
19. Velasco-Miguel S,Buckbinder L,Jean P,et al. PA26, a novel target of the p53 tumor suppressor and member of the GADD family of DNA damage and growth arrest inducible genesOncogeneYear: 199918127379926927
20. Matsuzawa S,Takayama S,Froesch BA,et al. p53-inducible human homogue of Drosophila seven in absentia (Siah) inhibits cells growth: suppression by BAG-1EMBO JYear: 1998172736479582267
21. Nemani M,Linares-Cruz G,Bruzzoni-Giovanelli H,et al. Activation of the human homologue of the Drosophila sina gene in apoptosis and tumor suppressionProc Natl Acad Sci U S AYear: 1996939039428799150
22. Hermeking H,Lengauer C,Polyak K,et al. 14-3-3 sigma is a p53-regulated inhibitor of G2/M progressionMol CellYear: 199713119659898
23. Ashkenazi A,Dixit VM. Death receptors: Signaling and modulationScienceYear: 1998281130589721089
24. Sun Y,Wicha M,Leopold WR. Regulation of metastasis-related gene expression by p53: a potential clinical implicationMol CarcinogYear: 19992425810029407
25. Cairns CA,White RJ. p53 is a general repressor of RNA polymerase III transcriptionEMBO JYear: 1998173112239606193
26. Lomax ME,Barnes DM,Hupp TR,et al. Characterization of p53 oligomerization domain mutations isolated from Li-Fraumeni and Li-Fraumeni like family membersOncogeneYear: 19981764399704930
27. Wu X,Webster SR,Chen J. Characterization of tumor-associated Chk2 mutationsJ Biol ChemYear: 20012762971411053450
28. Strauss EA,Hosler MR,Herzog P,et al. Complex replication error causes p53 mutation in a Li-Fraumeni familyCancer ResYear: 1995553237417614454
29. Ghaderi R. Mutations of p53 Gene in Skin Cancers: a Case Control StudyIran J Med SciYear: 20073258
30. Lee SB,Kim SH,Bell DW,et al. Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni SyndromeCancer ResYear: 2001618062711719428
31. Vahteristo P,Tamminen A,Karvinen P,et al. p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: further evidence of CHK2 in inherited cancer predispositionCancer ResYear: 20016157182211479205
32. Liang H,Atkins H,et al. Genomic organisation of the human MDM2 oncogene and relationship to its alternatively spliced mRNAsGeneYear: 20043382172315315825
33. Wu X,Bayle JH,Olson D,Levine AJ. The p53-mdm-2 autoregulatory feedback loopGenes DevYear: 199371126328319905
34. Vassilev LT. MDM2 inhibitors for cancer therapyTrends Mol MedYear: 200713233117126603
35. Vousden KH. Activation of the p53 tumor suppressor proteinBiochem Biophys ActaYear: 20021602475911960694
36. Vogelstein B,Lane D,Levine AJ. Surfing the p53 networkNatureYear: 20004083071011099028
37. Zheng H,You H,Zhou XZ,et al. The prolyl isomerase Pin1 is a regulator of p53 in genotoxic responseNatureYear: 20024198495312397361
38. Zacchi P,Gostissa M,Uchida T,et al. The prolyl isomerase Pin1 reveals a mechanism to control p53 functions after genotoxic insultsNatureYear: 2002419853712397362
39. Wulf GM,Liou YC,Ryo A,et al. Role of Pin1 in the regulation of p53 stability and p21 transactivation, and cell cycle checkpoints in response to DNA damageJ Biol ChemYear: 200227747976912388558
40. Giono LE,Manfredi JJ. Mdm2 plays a positive role as an effector of p53-dependent responsesCell CycleYear: 200762143717786043
41. Goldstein I,Marcel V,Olivier M,et al. Understanding wild-type and mutant p53 activities in human cancer: new landmarks on the way to targeted therapiesCancer GeneTherYear: 201118211
42. Stoklsa T,Golab J. Prospects for p53-based cancer therapyActa Biochim PolYear: 200552321815990917
43. He L,He X,Lim LP,et al. A microRNA component of the p53 tumour suppressor networkNatureYear: 20074471130417554337
44. Suzuki HI,Yamagata K,Sugimoto K,et al. Modulation of microRNA processing by p53NatureYear: 20094605293319626115
45. Chang TC,Wentzel EA,Kent OA,et al. Transactivation of miR-34a by p53 broadly influences gene expression and promotes apoptosisMol CellYear: 2007267455217540599
46. Afanasyeva EA,Mestdagh P,Kumps C,et al. MicroRNA miR-885-5p targets CDK2 and MCM5, activates p53 and inhibits proliferation and survivalCell Death DifferYear: 2011189748421233845

Article Categories:
  • Review Article

Keywords: Key Words TP53, CHK1, CHK2, MDM2, Li-Fraumeni syndrome, tumor suppressor.

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