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Article

Copy number variations of chromosome 17p13.1 might be linked to high risk of lung cancer in heavy smokers.

Molecular biology reports - 1 Nov 2011

Lee Minhyeok, Lee Yeiwon, Cho Hyun-Jung, Hong Jeeyoung, Kwon Sun-Jung, Park Chang-Gyo, Lee Hoi-Young, Son Ji-Woong, Kang Jaeku

Abstract excerpt

Lung cancer is the most common cause of cancer death worldwide. Smoking is known as the strongest single factor in the development of lung cancer. However, there are inherited genetic factors that cause different responses to cigarette smoking exposure among individuals. We tried to identify these differences in heavy smokers by examining copy number variations (CNVs) between lung cancer patients and healthy...

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Share to Chromosomes, Human, Pair 17
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21203850
DOI: 10.1007/s11033-010-0672-3

Genes

KCTD11
FGF11
PTPRH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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