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Please use this identifier to cite or link to this item: https://scholars.lib.ntu.edu.tw/handle/123456789/505135
Title: Genetic Load and Potential Mutational Meltdown in Cancer Cell Populations
Authors: Zhang Y.
Li Y.
Li T.
Shen X.
Zhu T.
Tao Y.
Li X.
Wang D.
Ma Q.
Hu Z.
Liu J.
Ruan J.
Cai J.
HURNG-YI WANG 
Lu X.
Keywords: copy number variation; genetic load; HeLa cell line; Muller's ratchet
Issue Date: 2019
Publisher: Oxford University Press
Journal Volume: 36
Journal Issue: 3
Start page/Pages: 541-552
Source: Molecular Biology and Evolution
Abstract: 
Large genomes with elevated mutation rates are prone to accumulating deleterious mutations more rapidly than natural selection can purge (Muller's ratchet). As a consequence, it may lead to the extinction of small populations. Relative to most unicellular organisms, cancer cells, with large and nonrecombining genome and high mutation rate, could be particularly susceptible to such "mutational meltdown." However, the most common type of mutation in organismal evolution, namely, deleterious mutation, has received relatively little attention in the cancer biology literature. Here, by monitoring single-cell clones from HeLa cell lines, we characterize deleterious mutations that retard the rate of cell proliferation. The main mutation events are copy number variations (CNVs), which, estimated from fitness data, happen at a rate of 0.29 event per cell division on average. The mean fitness reduction, estimated reaching 18% per mutation, is very high. HeLa cell populations therefore have very substantial genetic load and, at this level, natural population would likely face mutational meltdown. We suspect that HeLa cell populations may avoid extinction only after the population size becomes large enough. Because CNVs are common in most cell lines and tumor tissues, the observations hint at cancer cells' vulnerability, which could be exploited by therapeutic strategies. ? The Author(s) 2019.
URI: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85062168100&doi=10.1093%2fmolbev%2fmsy231&partnerID=40&md5=4025f5b4c88cb16e7f9a1cb91070c5e1
https://scholars.lib.ntu.edu.tw/handle/123456789/505135
ISSN: 0737-4038
DOI: 10.1093/molbev/msy231
SDG/Keyword: article; cancer cell; cell clone; cell division; cell line; cell population; cell proliferation; controlled study; copy number variation; gene mutation; genetic load; human; human cell; monitoring; natural population; population size; biological model; genetics; HeLa cell line; mutation; mutation accumulation; physiology; Cell Proliferation; DNA Copy Number Variations; Genetic Load; HeLa Cells; Humans; Models, Biological; Mutation; Mutation Accumulation; PC-3 Cells
[SDGs]SDG3
Appears in Collections:免疫學研究所

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臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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