Association of Hck genetic polymorphisms with gene expression and COPD

Xiaozhu Zhang, Salahaddin Mahmudi-Azer, John E. Connett, Nicholas R. Anthonisen, Jian Qing He, Peter D. Paré, Andrew J. Sandford

Research output: Contribution to journalArticlepeer-review

13 Scopus citations


Polymorphonuclear leukocytes (PMNs) are major effector cells in the chronic airway inflammation in chronic obstructive pulmonary disease (COPD). PMN degranulation is associated with degradation of extracellular matrix and tissue damage. Hck is an essential molecule in the signaling pathway regulating PMN degranulation. We hypothesized that polymorphisms affect the expression level of Hck, which, in turn, modulates PMN mediator release and tissue damage and influences the development of COPD. Here we systematically investigated genetic tag polymorphisms of the Hck gene, Hck mRNA and protein expression pattern in PMNs, and PMN mediator release (myeloperoxidase) in 60 healthy white subjects, and assessed their association with the use of several genetic models. The association of genetic polymorphisms with COPD-related phenotypes was determined in the lung healthy study cohort (LHS). We identified a novel 15 bp insertion/deletion polymorphism (8,656 L/S) in intron 1 of the Hck gene, which was associated with differential expression of Hck protein and PMN myeloperoxidase release. In the LHS cohort, there was significant interaction between the 8,656 L/S polymorphism and smoking on baseline lung function and 8,656 L/S was associated with bronchodilator response. These data suggest that the insertion/deletion polymorphism could be a functional polymorphism of the Hck gene, may contribute to COPD pathogenesis and modify COPD-related phenotypes.

Original languageEnglish (US)
Pages (from-to)681-690
Number of pages10
JournalHuman Genetics
Issue number5
StatePublished - Jan 2007

Bibliographical note

Funding Information:
Acknowledgments This study was supported by grants from the American Thoracic Society, the British Columbia Lung Association and by the National Institutes of Heath Grant 5R01HL064068–04. The authors gratefully acknowledge the NHLBI for the recruitment and characterization of this cohort Lung Health Study. AJS is the recipient of a Canada Research Chair in genetics.


  • COPD
  • Gene expression
  • Genetic polymorphism
  • Hck


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