Heteroplasmy of mutant mitochondrial DNA A10398G and analysis of its prognostic value in non-small cell lung cancer
Qi, Yuexiao ; Wei, Yuehua ; Wang, Qiaoli LU
; Xu, Hui
; Wang, You
; Yao, Anqi
; Yang, Hui
; Gao, Yan
and Zhou, Fuxiang
(2016)
In Oncology Letters
12(5).
p.3081-3088
- Abstract
Mitochondrial dysfunction is associated with pathogenic mitochondrial (mt)DNA mutations. The majority of mtDNA point mutations have a heteroplasmic status, which is defined as the coexistence of wild-type and mutated DNA within a cell or tissue. Previous findings demonstrated that certain mtDNA heteroplasmic mutations contribute to widely spread chronic diseases, including cancer, and alterations in the heteroplasmy level are associated with the clinical phenotype and severity of cancer. In the present study, the proportions of mutant mtDNA 10398G were assessed using amplification-refractory mutation system-quantitative polymerase chain reaction (PCR) assay in 129 non-small cell lung cancer (NSCLC) tissue samples. Wild-type and mutant... (More)
Mitochondrial dysfunction is associated with pathogenic mitochondrial (mt)DNA mutations. The majority of mtDNA point mutations have a heteroplasmic status, which is defined as the coexistence of wild-type and mutated DNA within a cell or tissue. Previous findings demonstrated that certain mtDNA heteroplasmic mutations contribute to widely spread chronic diseases, including cancer, and alterations in the heteroplasmy level are associated with the clinical phenotype and severity of cancer. In the present study, the proportions of mutant mtDNA 10398G were assessed using amplification-refractory mutation system-quantitative polymerase chain reaction (PCR) assay in 129 non-small cell lung cancer (NSCLC) tissue samples. Wild-type and mutant sequences were separately amplified using allele-specific primers and, subsequently, the PCR products containing the mtDNA 10398 site were ligated into vectors to construct a standard plasmid DNA construct. The association between mtDNA A10398G and the prognosis of patients was analyzed by survival analysis and Cox proportional hazards model. For the patient cohort, the median follow-up time and overall survival time were 20.6 and 26.3 months, respectively. The ratios of mutant heteroplasmy ranged between 0.31 and 97.04%. Patients with a high degree of mutant mtDNA 10398G had a significantly longer overall survival time compared with those with a low degree of mutant mtDNA 10398G (28.7 vs. 22.5 months, respectively; P<0.05). In addition, multivariate analysis demonstrated that epidermal growth factor receptor mutation status, tumor stage and the possession of a low degree of mutant 10398G were the three most independent prognostic factors. In conclusion, the present study suggests that, among NSCLC patients, there are large shifts in mutant mtDNA 10398G heteroplasmy and a low degree of mutant mtDNA 10398G heteroplasmy may be a marker of poor prognosis in patients with NSCLC.
(Less)
- author
- Qi, Yuexiao
; Wei, Yuehua
; Wang, Qiaoli
LU
; Xu, Hui
; Wang, You
; Yao, Anqi
; Yang, Hui
; Gao, Yan
and Zhou, Fuxiang
- publishing date
- 2016-11
- type
- Contribution to journal
- publication status
- published
- in
- Oncology Letters
- volume
- 12
- issue
- 5
- pages
- 3081 - 3088
- publisher
- Spandidos Publications
- external identifiers
-
- pmid:27899967
- scopus:84990031685
- ISSN
- 1792-1074
- DOI
- 10.3892/ol.2016.5086
- language
- English
- LU publication?
- no
- id
- d70c4bb6-03bc-4c7d-9144-b2c5703b5a28
- date added to LUP
- 2025-05-12 16:57:46
- date last changed
- 2025-06-24 07:46:22
@article{d70c4bb6-03bc-4c7d-9144-b2c5703b5a28,
abstract = {{<p>Mitochondrial dysfunction is associated with pathogenic mitochondrial (mt)DNA mutations. The majority of mtDNA point mutations have a heteroplasmic status, which is defined as the coexistence of wild-type and mutated DNA within a cell or tissue. Previous findings demonstrated that certain mtDNA heteroplasmic mutations contribute to widely spread chronic diseases, including cancer, and alterations in the heteroplasmy level are associated with the clinical phenotype and severity of cancer. In the present study, the proportions of mutant mtDNA 10398G were assessed using amplification-refractory mutation system-quantitative polymerase chain reaction (PCR) assay in 129 non-small cell lung cancer (NSCLC) tissue samples. Wild-type and mutant sequences were separately amplified using allele-specific primers and, subsequently, the PCR products containing the mtDNA 10398 site were ligated into vectors to construct a standard plasmid DNA construct. The association between mtDNA A10398G and the prognosis of patients was analyzed by survival analysis and Cox proportional hazards model. For the patient cohort, the median follow-up time and overall survival time were 20.6 and 26.3 months, respectively. The ratios of mutant heteroplasmy ranged between 0.31 and 97.04%. Patients with a high degree of mutant mtDNA 10398G had a significantly longer overall survival time compared with those with a low degree of mutant mtDNA 10398G (28.7 vs. 22.5 months, respectively; P<0.05). In addition, multivariate analysis demonstrated that epidermal growth factor receptor mutation status, tumor stage and the possession of a low degree of mutant 10398G were the three most independent prognostic factors. In conclusion, the present study suggests that, among NSCLC patients, there are large shifts in mutant mtDNA 10398G heteroplasmy and a low degree of mutant mtDNA 10398G heteroplasmy may be a marker of poor prognosis in patients with NSCLC.</p>}},
author = {{Qi, Yuexiao and Wei, Yuehua and Wang, Qiaoli and Xu, Hui and Wang, You and Yao, Anqi and Yang, Hui and Gao, Yan and Zhou, Fuxiang}},
issn = {{1792-1074}},
language = {{eng}},
number = {{5}},
pages = {{3081--3088}},
publisher = {{Spandidos Publications}},
series = {{Oncology Letters}},
title = {{Heteroplasmy of mutant mitochondrial DNA A10398G and analysis of its prognostic value in non-small cell lung cancer}},
url = {{http://dx.doi.org/10.3892/ol.2016.5086}},
doi = {{10.3892/ol.2016.5086}},
volume = {{12}},
year = {{2016}},
}