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一名前列腺癌患者线粒体 COI 基因中存在的遗传异质性突变改变了活性氧、活性氮和增殖。

An inherited heteroplasmic mutation in mitochondrial gene COI in a patient with prostate cancer alters reactive oxygen, reactive nitrogen and proliferation.

机构信息

Department of Urology, School of Medicine, Emory University, 1365 Clifton Rd. Building B, Atlanta, GA 30322, USA.

出版信息

Biomed Res Int. 2013;2013:239257. doi: 10.1155/2013/239257. Epub 2012 Dec 27.

DOI:10.1155/2013/239257
PMID:23509693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3591245/
Abstract

Mitochondrial DNA (mtDNA) mutations have been found in many cancers but the physiological derangements caused by such mutations have remained elusive. Prostate cancer is associated with both inherited and somatic mutations in the cytochrome c oxidase (COI) gene. We present a prostate cancer patient-derived rare heteroplasmic mutation of this gene, part of mitochondrial respiratory complex IV. Functional studies indicate that this mutation leads to the simultaneous decrease in cytochrome oxidation, increase in reactive oxygen, and increased reactive nitrogen. These data suggest that mitochondrial DNA mutations resulting in increased reactive oxygen and reactive nitrogen generation may be involved in prostate cancer biology.

摘要

线粒体 DNA(mtDNA)突变已在许多癌症中被发现,但此类突变引起的生理紊乱仍难以捉摸。前列腺癌与细胞色素 c 氧化酶(COI)基因的遗传和体细胞突变有关。我们报告了一例前列腺癌患者的该基因部分线粒体呼吸复合物 IV 的罕见异质突变。功能研究表明,该突变导致细胞色素氧化同时减少、活性氧增加和活性氮增加。这些数据表明,导致活性氧和活性氮生成增加的线粒体 DNA 突变可能参与前列腺癌生物学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/b0123e96a77c/BMRI2013-239257.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/2e3b1ebf8f1b/BMRI2013-239257.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/0447e112c972/BMRI2013-239257.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/e500a6994ae9/BMRI2013-239257.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/e3a9cb0b4828/BMRI2013-239257.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/d41454f4ab7c/BMRI2013-239257.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/b0123e96a77c/BMRI2013-239257.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/2e3b1ebf8f1b/BMRI2013-239257.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/0447e112c972/BMRI2013-239257.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/e500a6994ae9/BMRI2013-239257.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/e3a9cb0b4828/BMRI2013-239257.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/d41454f4ab7c/BMRI2013-239257.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecff/3591245/b0123e96a77c/BMRI2013-239257.006.jpg

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Nitric oxide: role in tumour biology and iNOS/NO-based anticancer therapies.一氧化氮:在肿瘤生物学和 iNOS/NO 为基础的抗癌治疗中的作用。
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Pathogenic mitochondrial DNA mutations inhibit melanoma metastasis.致病性线粒体 DNA 突变抑制黑色素瘤转移。
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