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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Mitochondrial genome instability in colorectal adenoma and adenocarcinoma

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Author(s):
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de Araujo, Luiza F. [1, 2] ; Fonseca, Aline S. [1, 2] ; Muys, Bruna R. [1, 2] ; Placa, Jessica R. [2] ; Bueno, Rafaela B. L. [1, 2] ; Lorenzi, Julio C. C. [1, 2] ; Santos, Anemari R. D. [2] ; Molfetta, Greice A. [1, 2, 3] ; Zanette, Dalila L. [1, 2, 3] ; Souza, Jorge E. S. [2, 3] ; Valente, Valeria [2, 3, 4] ; Silva, Jr., Wilson A. [1, 2, 3]
Total Authors: 12
Affiliation:
[1] Univ Sao Paulo, Dept Genet, Ribeirao Preto Med Sch, BR-14049 Ribeirao Preto - Brazil
[2] CNPq, Natl Inst Sci & Technol Stem Cell & Cell Therapy, Ctr Cell Based Therapy CEPID FAPESP, Reg Blood Ctr Ribeirao Preto, Ribeirao Preto - Brazil
[3] Ctr Integrat Syst Biol CISBi NAP USP, Ctr Med Genom HCFMRP USP, Ribeirao Preto - Brazil
[4] Univ Sao Paulo State, Fac Pharmaceut Sci Araraquara, Dept Clin Anal, Araraquara - Brazil
Total Affiliations: 4
Document type: Journal article
Source: TUMOR BIOLOGY; v. 36, n. 11, p. 8869-8879, NOV 2015.
Web of Science Citations: 10
Abstract

Mitochondrial dysfunction is regarded as a hallmark of cancer progression. In the current study, we evaluated mitochondrial genome instability and copy number in colorectal cancer using Next Generation Sequencing approach and qPCR, respectively. The results revealed higher levels of heteroplasmy and depletion of the relative mtDNA copy number in colorectal adenocarcinoma. Adenocarcinoma samples also presented an increased number of mutations in nuclear genes encoding proteins which functions are related with mitochondria fusion, fission and localization. Moreover, we found a set of mitochondrial and nuclear genes, which cooperate in the same mitochondrial function simultaneously mutated in adenocarcinoma. In summary, these results support an important role for mitochondrial function and genomic instability in colorectal tumorigenesis. (AU)

FAPESP's process: 08/57877-3 - National Institute of Science and Technology in Cell Therapy
Grantee:Roberto Passetto Falcão
Support type: Research Projects - Thematic Grants
FAPESP's process: 13/08135-2 - CTC - Center for Cell-Based Therapy
Grantee:Dimas Tadeu Covas
Support type: Research Grants - Research, Innovation and Dissemination Centers - RIDC