TP53 codon 72 polymorphism and type 2 diabetes: a case-control study in South Indian population

被引:6
作者
Punja, Harshitha K. [1 ]
Nanjappa, Dechamma Pandyanda [2 ]
Babu, Nishith [2 ]
Kalladka, Krithika [2 ]
Shanti Priya Dias, B. [2 ]
Chakraborty, Gunimala [2 ]
Rao, Sudhindra M. [1 ]
Chakraborty, Anirban [2 ]
机构
[1] Nitte, KS Hegde Med Acad, Dept Gen Med, Mangaluru 575018, India
[2] Nitte, Nitte Univ Ctr Sci Educ & Res NUCSER, Div Mol Genet & Canc, Kotekar Beeri Rd, Mangaluru 575018, India
关键词
Tumor protein p53; Metabolic disorder; Genetic alterations; Insulin resistance; Indian cohort; P53; TRANSACTIVATION;
D O I
10.1007/s11033-021-06505-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
TP53 functions primarily as a tumor suppressor, controlling a myriad of signalling pathways that prevent a cell from undergoing malignant transformation. This tumor suppressive function requires an activation and stabilization of TP53 in response to cell stressors. However, besides its cancer-preventive functions, TP53 is also known to be involved in diverse cellular processes including metabolism, reproduction, stem cell renewal and development. Indeed, several lines of evidence strongly suggest that TP53 plays crucial role in diabetes. A number of studies have evaluated the association of genetic alterations (single nucleotide variations) in TP53 gene with the development of diabetes. However, the results have not been consistent. The aim of this study was to evaluate whether the C/G polymorphism at codon 72 (Pro72/Arg72), located in exon 4 of TP53, is associated with type 2 diabetes in South Indian population. A total of 74 type 2 diabetic patients and 54 non-diabetic subjects were screened. None of the three genotypes, namely C/C (Pro/Pro), C/G (Pro/Arg), and G/G (Arg/Arg) was found to be significantly associated with type 2 diabetes in our study group. The findings of this study indicate that TP53 codon 72 polymorphism is not associated with increased risk of type 2 diabetes in South Indian population. Further studies with a large cohort size would be necessary to corroborate the observations of this study. Nevertheless, this study represents the first genetic analysis of TP53 variants in South Indian type 2 diabetic patients.
引用
收藏
页码:5093 / 5097
页数:5
相关论文
共 23 条
  • [1] Requirement of the ATM/p53 Tumor Suppressor Pathway for Glucose Homeostasis
    Armata, Heather L.
    Golebiowski, Diane
    Jung, Dae Young
    Ko, Hwi Jin
    Kim, Jason K.
    Sluss, Hayla K.
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2010, 30 (24) : 5787 - 5794
  • [2] Bitti MLM, 2010, J PEDIATR ENDOCR MET, V23, P291
  • [3] Genotypes of p53 codon 72 correlate with age at onset of type 1 diabetes in a sex-specific manner
    Bitti, Maria Luisa Manca
    Saccucci, Patrizia
    Capasso, Francesca
    Piccinini, Simona
    Angelini, Federica
    Rapini, Novella
    Porcari, Marta
    Arcano, Susanna
    Petrelli, Arianna
    Del Duca, Elisabetta
    Bottini, Egidio
    Gloria-Bottini, Fulvia
    [J]. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2011, 24 (7-8) : 437 - 439
  • [4] The p53 codon 72 (Arg72Pro) polymorphism is associated with the degree of insulin resistance in type 2 diabetic subjects: a cross-sectional study
    Bonfigli, Anna Rita
    Sirolla, Cristina
    Testa, Roberto
    Cucchi, Michela
    Spazzafumo, Liana
    Salvioli, Stefano
    Ceriello, Antonio
    Olivieri, Fabiola
    Festa, Roberto
    Procopio, Antonio Domenico
    Brandoni, Gabriele
    Boemi, Massimo
    Marra, Maurizio
    Franceschi, Claudio
    [J]. ACTA DIABETOLOGICA, 2013, 50 (03) : 429 - 436
  • [5] The pathobiology of diabetic complications - A unifying mechanism
    Brownlee, M
    [J]. DIABETES, 2005, 54 (06) : 1615 - 1625
  • [6] Studies of the Association of Arg72Pro of Tumor Suppressor Protein p53 with Type 2 Diabetes in a Combined Analysis of 55,521 Europeans
    Burgdorf, Kristoffer Solvsten
    Grarup, Niels
    Justesen, Johanne Marie
    Harder, Marie Neergaard
    Witte, Daniel Rinse
    Jorgensen, Torben
    Sandbaek, Annelli
    Lauritzen, Torsten
    Madsbad, Sten
    Hansen, Torben
    Pedersen, Oluf
    [J]. PLOS ONE, 2011, 6 (01):
  • [7] Guarding the 'translation apparatus': defective ribosome biogenesis and the p53 signaling pathway
    Chakraborty, Anirban
    Uechi, Tamayo
    Kenmochi, Naoya
    [J]. WILEY INTERDISCIPLINARY REVIEWS-RNA, 2011, 2 (04) : 507 - 522
  • [8] The codon 72 polymorphic variants of p53 have markedly different apoptotic potential
    Dumont, P
    Leu, JIJ
    Della Pietra, AC
    George, DL
    Murphy, M
    [J]. NATURE GENETICS, 2003, 33 (03) : 357 - 365
  • [9] Glucose Tolerance in Mice is Linked to the Dose of the p53 Transactivation Domain
    Franck, Debra
    Tracy, Laura
    Armata, Heather L.
    Delaney, Christine L.
    Jung, Dae Young
    Ko, Hwi Jin
    Ong, Helena
    Kim, Jason K.
    Scrable, Heidi
    Sluss, Hayla K.
    [J]. ENDOCRINE RESEARCH, 2013, 38 (03) : 139 - 150
  • [10] Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes
    Gaulton, Kyle J.
    Willer, Cristen J.
    Li, Yun
    Scott, Laura J.
    Conneely, Karen N.
    Jackson, Anne U.
    Duren, William L.
    Chines, Peter S.
    Narisu, Narisu
    Bonnycastle, Lori L.
    Luo, Jingchun
    Tong, Maurine
    Sprau, Andrew G.
    Pugh, Elizabeth W.
    Doheny, Kimberly F.
    Valle, Timo T.
    Abecasis, Goncalo R.
    Tuomilehto, Jaakko
    Bergman, Richard N.
    Collins, Francis S.
    Boehnke, Michael
    Mohlkel, Karen L.
    [J]. DIABETES, 2008, 57 (11) : 3136 - 3144