Skip to content

Advertisement

BMC Cancer

What do you think about BMC? Take part in

Open Access
Open Peer Review

This article has Open Peer Review reports available.

How does Open Peer Review work?

Association of the germline TP53R337H mutation with breast cancer in southern Brazil

  • Juliana G Assumpção1,
  • Ana Luíza Seidinger1,
  • Maria José Mastellaro1,
  • Raul C Ribeiro2, 3,
  • Gerard P Zambetti4,
  • Ramapriya Ganti5,
  • Kumar Srivastava6,
  • Sheila Shurtleff5,
  • Deqing Pei6,
  • Luiz Carlos Zeferino7,
  • Rozany M Dufloth8,
  • Silvia Regina Brandalise1 and
  • José Andres Yunes1Email author
BMC Cancer20088:357

https://doi.org/10.1186/1471-2407-8-357

Received: 01 July 2008

Accepted: 01 December 2008

Published: 01 December 2008

Abstract

Background

The germline TP53-R337H mutation is strongly associated with pediatric adrenocortical tumors (ACT) in southern Brazil; it has low penetrance and limited tissue specificity in most families and therefore is not associated with Li-Fraumeni syndrome. However, other tumor types, mainly breast cancer, have been observed in carriers of several unrelated kindreds, raising the possibility that the R337H mutation may also contribute to breast tumorigenesis in a genetic background-specific context.

Methods

We conducted a case-control study to determine the prevalence of the R337H mutation by sequencing TP53 exon 10 in 123 women with breast cancer and 223 age- and sex-matched control subjects from southern Brazil. Fisher's test was used to compare the prevalence of the R337H.

Results

The R337H mutation was found in three patients but in none of the controls (p = 0.0442). Among the carriers, two had familial history of cancer meeting the Li-Fraumeni-like criteria. Remarkably, tumors in each of these three cases underwent loss of heterozygosity by eliminating the mutant TP53 allele rather than the wild-type allele. Polymorphisms were identified within the TP53 (R72P and Ins16) and MDM2 (SNP309) genes that may further diminish TP53 tumor suppressor activity.

Conclusion

These results demonstrate that the R337H mutation can significantly increase the risk of breast cancer in carriers, which likely depends on additional cooperating genetic factors. These findings are also important for understanding how low-penetrant mutant TP53 alleles can differentially influence tumor susceptibility.

Introduction

Mutations in the TP53 tumor supressor gene usually occur within the highly conserved DNA-binding domain (aa 100–298) and, when inherited, are typically associated with Li-Fraumeni syndrome (LFS), in which carriers develop a broad spectrum of cancers (e.g., breast, brain, soft tissue, bone, blood, and adrenal cortex tumors) during childhood or young adulthood [1]. Families with incomplete features of LFS are referred to as having Li-Fraumeni-like (LFL) syndrome [2, 3].

In southern Brazil, a unique germline TP53 point mutation resulting in an Arg to His amino acid substitution (R337H) within the C-terminal oligomerization domain is strongly associated with childhood adrenocortical tumors (ACT) [46]. Unlike the protypical DNA binding mutants, p53-R337H retains significant activity, although its thermal stability is reduced and it is highly sensitive to slight changes in pH [7]. The R337H mutation has a low overall malignant potential but is remarkably organ-specific, affecting mainly the adrenal cortex [4].

In most southern Brazilian families bearing the R337H mutation, pediatric ACT is the only malignancy observed [46]. However, in about 10–20% of the cases [[6], Seidinger et al., manuscript in preparation] the family cancer history fulfills the criteria for LFL syndrome with breast cancer being one of the most common malignancies [6]. Achatz and coworkers [8] identified R337H carriers among Brazilian LFL families, including one case of breast carcinoma that underwent loss of the wild-type allele and retained the mutant allele. These observations suggested that the R337H mutation may play a role in breast tumorigenesis. To test whether the R337H is associated with breast cancer, we retrospectively examined the prevalence of the mutation in a group of Brazilian women with breast cancer.

Methods

Patients and Clinical Data

The study group comprised 123 women with breast cancer that had been diagnosed and treated at the Hospital of the State University of Campinas (CAISM/UNICAMP), São Paulo, Brazil. The patient's cohort consisted of a subgroup of women who presented a familial history of breast cancer (n = 45) and another subgroup consisted of sporadic breast cancer cases (n = 78). The criteria for the selection of individuals with familial history were: more than three cases of breast cancer and more than one case of ovarian cancer in the family; more than two first-degree relatives with breast cancer; one case of male breast cancer [9, 10]. Thirty of the 45 patients with positive familial history were previously tested for BRCA1/2 mutations [11]. A control group of 223 age-matched female volunteers was selected among university personnel. Family cancer history and blood samples were obtained with informed consent under the guidelines and approval of the Ethical Research Committees of the Faculty of Medical Sciences (FCM) at UNICAMP and The Centro Infantil Boldrini, and the National Committee of Ethics in Research (CONEP). Aditional clinical information, slides and paraffin blocks were obtained for those patients who were shown to carry the R337H mutation.

DNA analysis

Genomic DNA was isolated from peripheral blood by using a standard phenol-chloroform extraction method [12]. Paraffin-embedded tumor samples were treated with xylene-100% ethanol (1:1) and digested with proteinase K (14 mg/mL) in 50 mmol/L Tris-HCl (pH 8.0) before phenol-chloroform extraction.

TP53 exon 10 was amplified by using primers and PCR conditions described by Figueiredo et al. [6], with the exception of the forward primer used for amplification of exon 10 DNA from tumor biopsies: 5'-CCATCTTTTAACTCAGGTACTG-3'. TP53 intron 3 and exon 4 were amplified by using primers 5'-CCCTAGCAGAGACCTGTGGGAA-3' (foward) and 5'-AGGCATTGAAGTCTCATGGAA-3'(reverse). TP53 PCR products were directly sequenced by using the BigDye terminator cycle sequencing ready reaction kit (Applied Biosystems, Foster City, CA) in an ABI PRISM 3700 automatic sequencer (Applied Biosystems). The sequences were compared to the human TP53 reference sequence (National Center for Biotechnology Information, accession number U94788). All mutations were confirmed by a second, independent analysis. Tumor DNA was also screened for TP53 alterations in other exons and introns where technically feasible, essentially as previously described [13]. In cases heterozygous for codon 72 and ins16, haplotypes were determined by performing an allele-specific PCR assay as described by Osorio et al. [14]. The MDM2 promoter was amplified with primers described by Bond et al. [15] and PCR products were analyzed by restriction fragment length polymorphism as described by Walsh et al. [16].

Immunohistochemistry

Expression of p53 protein was examined by immunohistochemistry with the DO7 monoclonal antibody (Dako) at 1:100 dilution. The slides were incubated with Envision labeled polymer components (Dako, K1491) and developed with 3-3-diaminobenzidine (Sigma, D5637). Tissue from borderline ovarian tumors was included in each assay as a positive control for p53. Slides were interpreted at 40× magnification by a single pathologist. p53 protein expression was considered positive when more than 10% of the nuclei were stained; staining intensity was not considered.

Statistical analysis

Fisher's exact test (FREQ procedures in SAS v9.1.3, SAS Institute Inc., Cary, NC) was used to compare the frequency of the R337H mutation in the breast cancer and control groups. The R337H mutation rate in the breast cancer group was estimated and the 95% exact CI reported. This rate was compared to the estimated population frequency of the mutation (assumed to be the true prevalence rate for the population) in the region of interest in southern Brazil by using the one-sided exact test for binomial proportion.

Results

Identification of the germline R337H TP53mutation in breast cancer patients

The R337H mutation was detected in the germline DNA of three of 123 breast cancer patients in southern Brazil. None of the 223 control subjects carried the R337H mutation or any other mutation in TP53 exon 10. There was a significant association between the presence of the R337H mutation and breast cancer (p = 0.0442; Fisher's exact test, Table 1). The mutation rate of R337H in the cancer-positive group was 2.4%, with an exact Blyth-Still-Casella 95% CI of 0.7% to 6.6%. The overall frequency of the R337H in the region of interest in southern Brazil is assumed to be in the range 0.2%–0.3% [[17], B. Figueiredo, personal communication]. Therefore, the frequency of the R337H mutation was significantly greater among patients with breast cancer than in the general population of the region (p = 0.002 and 0.006 in comparison to a population prevalence rate of 0.2% and 0.3%, respectively; one-sided exact binomial test).
Table 1

Relation of the R337H TP53 mutation to breast cancer status

Gene

Codon

Genotype

Cases (%)

Controls (%)

P value

TP53

337

Arg/Arg

120 (97.6%)

223 (100%)

0.0442

  

Arg/His

3 (2.4%)

0

 

Family cancer history

Table 2 summarizes clinical findings for the three carriers of the R337H mutation. All three developed breast cancer at an early age (19, 29, and 44 years). Patient 2 had a second cancer (brain tumor) at the age of 31 years. Patient 1 had no familial history of cancer. Patient 2 had two first-degree relatives with cancer; although the tumor type and age of onset were not known, this family might fulfill LFL-syndrome criteria. Patient 3's family cancer history met Birch's criteria [2] for LFL: a mother with bilateral breast cancer at age 53, three maternal aunts with post-menopausal breast-cancer, a sister with leukemia at age 48, and a grandson with adrenocortical carcinoma at age 18 months.
Table 2

Clinical findings and family cancer history of the three TP53 R337H carriers

Patient

Tumor Type

Age Onset

TP53 IHC

Family Cancer History

1

Breast; phyllodes, malignant

19 years

Negative

No cancer

2

Breast; invasive ductal carcinoma

Brain tumor (malignant)

29 years

31 years

Negative

Positive

Two first-degree relatives (1-U; 1-A)

3

Invasive ductal carcinoma

44 years

Positive

Six first-degree relatives (4-BC; 1-L; 1-ACC)

IHC = immunohistochemistry, U = uterus, A = arm (unknown type of cancer), BC = breast cancer, L = leukemia, ACC = adrenocortical carcinoma

Selection against the mutant TP53R337H allele during breast tumorigenesis

Tumors with a germline or somatic TP53 mutation usually experience loss of heterozygosity (LOH) in which the wild-type allele is deleted or mutated. Surprisingly, the mutant R337H allele was deleted in all three of the studied breast tumors. No somatic mutations were detected within sequences that could be determined (exons 2, 4, 5, 7, 8, 9, and 10) in any of the breast tumors. By contrast, the brain tumor of patient 2 was homozygous for the R337H TP53 mutation, it also had a second, acquired mutation (T125M), in the DNA binding domain.

Tumor expression of p53 protein

R337H-mutant protein accumulates within the nuclei of ACT cells and is detectable by immunohistochemistry, as is other missense mutant p53 expressed in tumors [4]. Breast tumor tissue from patients 1 and 2 was negative for nuclear p53, consistent with selection against the mutant allele. However, breast tumor tissue from patient 3 expressed nuclear p53. Because this tumor had deleted the mutant allele (Table 2), this finding implies that a somatic TP53 mutation outside of exon 10 was acquired during tumorigenesis. However, insufficient tumor tissue hindered the identification of this genetic alteration. The brain tumor tissue from patient 2 also stained positive for nuclear p53, consistent with retention of the allele encoding 337H and acquisition of a second-site mutation (T125M) within the DNA binding domain (See additional file 1: IHC and LOH results of tumor samples from R337H patients).

Polymorphisms associated with the R337H mutation and breast cancer

To investigate whether TP53 polymorphisms were associated with the R337H mutation in the three breast tumor patients, we tested for two common TP53 variants (R72P and ins16) reported to affect breast cancer susceptibility [1821]. Patients 1 and 3 were heterozygous in the germline for both the R72P and ins16. Patient 2 was homozygous for R72 and negative for ins16 (Table 3). In the tumor tissue of patients 1 and 3, codon 72 encoded only arginine, indicating a selection against the proline allele.
Table 3

Germline and tumor genotype of TP53 and MDM2

Patient

DNA Sample

TP53 c 337

TP53 c72

TP53 Ins16

TP53 Haplotypes

MDM2-309

1

Blood

Arg/His

Arg/Pro

Ins+/Ins-

Arg;ins-/Pro;ins+

T/G

 

Breast Tumor

Arg

Arg

   

2

Blood

Arg/His

Arg/Arg

Ins-/Ins-

Arg;ins-/Arg;ins-

T/G

 

Breast Tumor

Arg

Arg

   
 

Brain Tumor

His

Arg

   

3

Blood

Arg/His

Arg/Pro

Ins+/Ins-

Arg;ins-/Pro;ins+

T/T

 

Breast Tumor

Arg

Arg

   

Due to early age of tumor onset, patient 1 was also tested for BRCA1/2 (data not shown) and a polymophic change was detected at BRCA2 exon 10 (N372H). The other two R337H carriers were not screened for BRCA1/2 mutations.

We also investigated the presence of the SNP309-G within the first intron of the MDM2 gene, which is a key negative regulator of p53 protein [22]. SNP309-G has been reported to accelerate tumor formation in carriers of a TP53 mutation [15]. Patients 1 and 2 were heterozygous for SNP309-G (G/T) and patient 3 was homozygous for the T allele (T/T) (Table 3).

Discussion

Our findings show that the germline TP53 R337H mutation is associated with breast cancer in southern Brazil within the context of LFL-like families and a sporadic case. In our case-control study, three (2.4%) breast cancer patients, but none of the age-matched control subjects, carried this mutation. This frequency is approximately 10 times that estimated in the general southern Brazilian population (0.2% to 0.3%; p = 0.0221) [[17], B. Figueiredo, personal communication].

Germline TP53 mutations are estimated to occur in no more than 0.25% of patients with breast tumors, regardless of family history [2325]. Therefore, the R337H mutation is the most common inherited TP53 mutation associated with breast cancer in southern Brazil. It is also the most frequently reported germline mutation in the International Agency for Research on Cancer database [26, 27], predominantly because of its association with most pediatric ACT cases (~80%–95%) in southern Brazil [4, 5]. However, the high incidence of breast cancer in this region is unlikely to be solely attributable to the R337H TP53 mutation, as only 2.4% of women with breast cancer in this cohort carried the mutation.

It remains unclear how the R337H mutation contributes to breast tumorigenesis. Remarkably, all three tumors selected against the mutant allele and retained the wild-type allele. In striking contrast, virtually all pediatric ACTs found to be associated with a germline R337H mutation had selected against the wild-type allele [4, 5], including that of the grandson of patient 3 (data not shown). These results suggest that the mechanism of R337H-associated ACT tumorigenesis differs from that of R337H-associated breast cancer. The R337H mutation appears to play a role in accelerating the onset of breast tumorigenesis, but may not affect tumor progression in some individuals, however further studies are required to clarify this matter.

Many families that carry the germline R337H mutation are selectively predisposed to childhood ACT [4, 6], although some appear to be at higher risk of more diverse cancers, including breast tumors and possibly other LF spectrum neoplasms such as brain tumors. Indeed, the R337H has been detected in LFL syndrome cases [8], but these represent the minority of the families positive for R337H [[6], Seidinger et al., manuscript in preparation]. We believe that the cancer predisposing character of low-penetrant TP53 mutations, such as R337H, depends on additional genetic modifiers.

Our observations of TP53 polymorphisms (R72P and ins16) and MDM2 (SNP309) are consistent with this hypothesis. Two out of the three R337H positive patients were heterozygous for the R72P and ins16 polymorphisms (Table 3). Although the consequence of these polymorphisms is controversial, proline-72 is proposed to function less well in triggering apoptosis and tumor suppression [28]. Likewise, ins16 within intron 3 diminishes TP53 expression [29] and has been implicated in ovarian and breast cancer [18, 30, 19, 31]. Patients 1 and 2 who were 19 and 29 years old at diagnosis, respectively, were heterozygous for MDM2 SNP309 (G/T), while patient 3 who was 44 years old at diagnosis, was homozygous for the T allele (T/T). These findings are in line with previous reports showing that individuals carrying a TP53 germline mutation who are heterozygous or homozygous for SNP309-G develop tumors on average 10 years earlier than carriers of TP53 mutations who lack SNP309 [15, 32]. Moreover, patient 1 also carries the N372H polymorphism at BRCA2 exon 10, which might contribute to breast tumorigenesis [33].

It is possible that the R337H mutation in combination with these polymorphisms and possibly other genetic alterations creates a p53-insufficient state that enhances tumor susceptibility. The degree of p53 function retained by a particular mutant and influenced by genetic modifiers within its signaling pathway dictates the level of tumor risk, which we refer to as the TP53 gradient effect [34].

In conclusion, we showed that the TP53R337H mutation is significantly associated with breast cancer in southern Brazil. However, this mutation is likely to account for only a small proportion of breast cancer cases in this region. Our results illustrate the complexity of constitutional predisposition to cancer, including that associated with TP53 mutations. A rigorous family history of cancer, p53 predicted functional characteristics, the presence of other genetic modifiers, and examination of the tumor cells for loss of heterozygosity must be considered in risk assessment analysis and genetic counseling.

Abbreviations

ACT: 

adrenocortical tumor

LFS: 

Li-Fraumeni syndrome

LFL: 

Li-Fraumeni-like

LOH: 

loss of heterozygosity

SNP: 

single nucleotide polymorphism

BRCA1/2: 

breast cancer genes 1 and 2.

Declarations

Acknowledgements

This work was supported by grants CA63230 and CA21765 from the National Institutes of Health, by the American Lebanese Syrian Associated Charities (ALSAC), and by grant 05-02390 from the Research Foundation of the State of Sao Paulo (FAPESP), Brazil.

We thank all research subjects for their cooperation. The authors also thank Dr. Carmen Bertuzzo (FCM/UNICAMP), the laboratory of Anatomia Patológica (FCM/UNICAMP) for technical support, C. Proffitt (SJCRH) for technical assistance, and Sharon Naron for editorial revision of the manuscript.

Authors’ Affiliations

(1)
Centro Infantil Boldrini
(2)
Department of Oncology, St. Jude Children's Research Hospital
(3)
International Outreach Program, St. Jude Children's Research Hospital
(4)
Department of Biochemistry, St. Jude Children's Research Hospital
(5)
Department of Pathology, St. Jude Children's Research Hospital
(6)
Department of Biostatistics, St. Jude Children's Research Hospital
(7)
Universidade Estadual de Campinas
(8)
Universidade Federal de Santa Catarina

References

  1. Malkin D, Li FP, Strong LC, Fraumeni JF, Nelson CE, Kim DH, Kassel J, Gryka MA, Bischoff FZ, Tainsky MA, Friend SH: Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science. 1990, 250: 1233-8. 10.1126/science.1978757.View ArticlePubMedGoogle Scholar
  2. Birch JM, Hartley AL, Tricker KJ, Prosser J, Condie A, Kelsey AM, Harris M, Jones PH, Binchy A, Crowther D, Craft AW, Eden OB, Evans GR, Thompson E, Mann JR, Martin J, Mitchell ELD, Santibánez-Koref MF: Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families. Cancer Res. 1994, 54: 1298-304.PubMedGoogle Scholar
  3. Eeles RA: Germline mutations in the TP53 gene. Cancer Surv. 1995, 25: 101-124.PubMedGoogle Scholar
  4. Ribeiro RC, Sandrini F, Figueiredo B, Zambetti G, Lafferty AR, DeLacerda L, Rabin M, Cadwell RC, Sampaio G, Cat I, Stratakis CA, Sandrini R: An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma. Proc Natl Acad Sci USA. 2001, 98: 9330-5. 10.1073/pnas.161479898.View ArticlePubMedPubMed CentralGoogle Scholar
  5. Latronico AC, Pinto EM, Domenice S, Fragoso MC, Martin RM, Zerbini MC, Lucon AM, Mendonca BB: An inherited mutation outside the highly conserved DNA-binding domain of the p53 tumor suppressor protein in children and adults with sporadic adrenocortical tumors. J Clin Endocrinol Metab. 2001, 86: 4970-3. 10.1210/jc.86.10.4970.View ArticlePubMedGoogle Scholar
  6. Figueiredo BC, Sandrini R, Zambetti GP, Pereira RM, Cheng C, Liu W, Lacerda L, Pianovski MA, Michalkiewicz E, Jenkins J, Rodrigues-Galindo C, Mastellaro MJ, Vianna S, Watanabe F, Sandrini F, Arram SBI, Boffetta P, Ribeiro RC: Penetrance of adrenocortical tumors associated with the germline TP53 R337H mutation. J Med Genet. 2006, 43: 91-96. 10.1136/jmg.2004.030551.View ArticlePubMedGoogle Scholar
  7. DiGiammarino EL, Lee AS, Cadwell C, Zhang W, Bothner B, Ribeiro RC, Zambetti G, Kriwacki RW: A novel mechanism of tumorigenesis involving pH-dependent destabilization of a mutant p53 tetramer. Nature Struct Biol. 2002, 9: 12-16. 10.1038/nsb730.View ArticlePubMedGoogle Scholar
  8. Achatz MIW, Olivier M, Le-Calvez F, Martel-Planche G, Lopes A, Rossi BM, Ashton-Prolla P, Giugliani E, Palmero EI, Vargas FR, da-Rocha JCC, Vettore AL, Hainaut P: The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families. Cancer Lett. 2007, 245: 96-102. 10.1016/j.canlet.2005.12.039.View ArticlePubMedGoogle Scholar
  9. Breast Cancer Linkage Consortium: Pathology of familial breast cancer: difference between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Lancet. 1997, 349: 1505-10. 10.1016/S0140-6736(96)10109-4.View ArticleGoogle Scholar
  10. Schimitt FC, Reis Filho JS, Milanezi F: Patología del cáncer de mama hereditario. Rev Senología y Patol Mam. 2001, 14: 29-35.Google Scholar
  11. Dufloth RM, Carvalho S, Heinrich JK, Shinzato JY, Santos CC, Zeferino LC, Schimitt F: Analysis of BRCA1 and BRCA2 mutations in Brazilian breast cancer patients with positive family history. Sao Paulo Med J. 2005, 123 (4): 192-197. 10.1590/S1516-31802005000400007.View ArticlePubMedGoogle Scholar
  12. Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning – A Laboratory Manual. 1989, Cold Spring Harbour Laboratoy Press, 2: 2Google Scholar
  13. West AN, Ribeiro RC, Jenkins J, Rodriguez-Galindo C, Figueiredo BC, Kriwacki R, Zambetti GP: Identification of a novel germ line variant hotspot mutant p53-R175L in pediatric adrenal cortical carcinoma. Cancer Res. 2006, 66: 5056-62. 10.1158/0008-5472.CAN-05-4580.View ArticlePubMedGoogle Scholar
  14. Osorio A, Martínez-Delgado B, Pollán M, Cuadros M, Urioste M, Torrenteras C, Melchor L, Díez O, De La Hoya M, Velasco E, González-Sarmiento R, Caldés T, Alonso C, Benítez J: A haplotype containing the p53 polymorphisms Ins16bp and Arg72Pro modifies cancer risk in BRCA2 mutation carriers. Hum Mutat. 2006, 27: 242-8. 10.1002/humu.20283.View ArticlePubMedGoogle Scholar
  15. Bond GL, Menin C, Hu W, Bond EE, Robins H, Lutzker SG, Arva NC, Bargonetti J, Bartel F, Taubert H, Wuerl P, Onel K, Yip L, Hwang SJ, Strong LC, Lozano G, Levine AJ: A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 Tumor Supressor pathway and accelerates tumor formation in humans. Cell. 2004, 119: 591-602. 10.1016/j.cell.2004.11.022.View ArticlePubMedGoogle Scholar
  16. Walsh CS, Miller CW, Karlan BY, Koeffler HP: Association between a functional single nucleotide polymorphism in the MDM2 gene and sporadic endometrial cancer risk. Gynecol Oncol. 2007, 104: 660-664. 10.1016/j.ygyno.2006.10.008.View ArticlePubMedGoogle Scholar
  17. Palmero EI, Schüler-Faccini L, Caleffi M, Achatz MI, Olivier M, Martel-Planche G, Marcel V, Aguiar E, Giacomazzi J, Ewald IP, Giugliani R, Hainaut P, Ashton-Prolla P: Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil. Cancer Lett. 2008, 261: 21-5. 10.1016/j.canlet.2007.10.044.View ArticlePubMedGoogle Scholar
  18. Wang-Gohrke S, Rebbeck TR, Besenfelder W, Kreienberg R, Runnebaum IB: p53 germline polymorphisms are associated with an increased risk for breast cancer in German women. Anticancer Res. 1998, 18: 2095-9.PubMedGoogle Scholar
  19. Wang-Gohrke S, Becher H, Kreienberg R, Runnebaum IB, Chang-Claude J: Intron 3 16 bp duplication polymorphism of p53 is associated with an increased risk for breast cancer by the age of 50 years. Pharmacogenetics. 2002, 12: 269-72. 10.1097/00008571-200204000-00012.View ArticlePubMedGoogle Scholar
  20. Tommiska J, Eerola H, Heinonen M, Salonen L, Kaare M, Tallila J, Ristimäki A, von Smitten K, Aittomäki K, Heikkilä P, Blomqvist C, Nevanlinna H: Breast cancer patients with p53 Pro72 homozygous genotype have a poorer survival. Clin Cancer Res. 2005, 11: 5098-103. 10.1158/1078-0432.CCR-05-0173.View ArticlePubMedGoogle Scholar
  21. Buyru N, Altinisik J, Demokan S, Dalay N: p53 genotypes and haplotypes associated with risk of breast cancer. Cancer Detect Prev. 2007, 31: 207-13. 10.1016/j.cdp.2007.04.004.View ArticlePubMedGoogle Scholar
  22. Momand J, Zambetti GP, Olson DC, George D, Levine AJ: The mdm-2 oncogene product forms a complex with the p53 protein and inhibits p53-mediated transactivation. Cell. 1992, 69: 1237-1245. 10.1016/0092-8674(92)90644-R.View ArticlePubMedGoogle Scholar
  23. Børresen AL, Andersen TI, Garber J, Barbier-Piraux N, Thorlacius S, Eyfjörd J, Ottestad L, Smith-Sørensen B, Hovig E, Malkin D, Friend SH: Screening for germ line TP53 mutations in breast cancer patients. Cancer Res. 1992, 52: 3234-6.PubMedGoogle Scholar
  24. Prosser J, Porter D, Coles C, Condie A, Thompson AM, Chetty U, Steel CM, Evans HJ: Constitutional p53 mutation in a non-Li-Fraumeni cancer family. Br J Cancer. 1992, 65: 527-8.View ArticlePubMedPubMed CentralGoogle Scholar
  25. Sidransky D, Tokino T, Helzlsouer K, Zehnbauer B, Rausch G, Shelton B, Prestigiacomo L, Vogelstein B, Davidson N: Inherited p53 gene mutations in breast cancer. Cancer Res. 1992, 52: 2984-6.PubMedGoogle Scholar
  26. International Agency for Research on Cancer (IARC): IARC TP53 database R12, November 2007. [http://www-p53.iarc.fr/index.html]
  27. Petitjean A, Mathe E, Kato S, Ishioka C, Tavtigian SV, Hainaut P, Olivier M: Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database. Hum Mutat. 2007, 28: 622-629. 10.1002/humu.20495.View ArticlePubMedGoogle Scholar
  28. Dumont P, Leu JI, Della Pietra AC, George DL, Murphy M: The codon 72 polymorphic variants of p53 have markedly different apoptotic potential. Nat Genet. 2003, 33: 357-365. 10.1038/ng1093.View ArticlePubMedGoogle Scholar
  29. Gemignani F, Moreno V, Landi S, Moullan N, Chabrier A, Gutiérrez-Enríquez S, Hall J, Guino E, Peinado MA, Capella G, Canzian F: A TP53 polymorphism is associated with increased risk of colorectal cancer and with reduced levels of TP53 mRNA. Oncogene. 2004, 23: 1954-6. 10.1038/sj.onc.1207305.View ArticlePubMedGoogle Scholar
  30. Wang-Gohrke S, Weikel W, Risch H, Vesprini D, Abrahamson J, Lerman C, Godwin A, Moslehi R, Olipade O, Brunet JS, Stickeler E, Kieback DG, Kreienberg R, Weber B, Narod SA, Runnebaum IB: Intron variants of the p53 gene are associated with increased risk for ovarian cancer but not in carriers of BRCA1 or BRCA2 germline mutations. Br J Cancer. 1999, 81: 179-183. 10.1038/sj.bjc.6690669.View ArticlePubMedPubMed CentralGoogle Scholar
  31. Costa S, Pinto D, Pereira D, Rodrigues H, Cameselle-Teijeiro J, Medeiros R, Schmitt F: Importance of TP53 codon 72 and intron 3 duplication 16 bp polymorphisms in prediction of susceptibility on breast cancer. BMC Cancer. 2008, 8: 32-10.1186/1471-2407-8-32.View ArticlePubMedPubMed CentralGoogle Scholar
  32. Ruijs MW, Schmidt MK, Nevanlinna H, Tommiska J, Aittomäki K, Pruntel R, Verhoef S, Van't Veer LJ: The single-nucleotide polymorphism 309 in the MDM2 gene contributes to the Li-Fraumeni syndrome and related phenotypes. Eur J Hum Genet. 2007, 15: 110-4. 10.1038/sj.ejhg.5201715.View ArticlePubMedGoogle Scholar
  33. Healey CS, Dunning AM, Teare MD, Chase D, Parker L, Burn J, Chang-Claude J, Mannermaa A, Kataja V, Huntsman DG, Pharoah PD, Luben RN, Easton DF, Ponder BA: A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability. Nat Genet. 2000, 26: 362-4. 10.1038/81691.View ArticlePubMedGoogle Scholar
  34. Zambetti GP: The p53 mutation "gradient effect" and its clinical implications. J Cell Physiol. 2007, 213: 370-373. 10.1002/jcp.21217.View ArticlePubMedGoogle Scholar
  35. Pre-publication history

    1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/8/357/prepub

Copyright

© Assumpção et al; licensee BioMed Central Ltd. 2008

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Advertisement