Epithelial cells obtained from buccal mucosa appear to have the same smoking-related molecular damage found in current sampling of bronchial epithelium
Epithelial cells from buccal mucosa may reliably reflect
smoking-related molecular damage in airway and pulmonary epithelium, allowing
patients to replace bronchoscopy with cheek swabbing, according to a presentation
at the annual meeting of the American Association for Cancer Research.
"We are talking about just a brushing inside of
the cheek to get the same information we would from lung brushings obtained through
bronchoscopy," said study presenter and lead author Manisha Bhutani, MD,
a post-doctoral fellow in Thoracic/Head and Neck Medical Oncology at the University
of Texas M. D. Anderson Cancer Center.
The team, led by senior researchers Li Mao, MD, examined
oral and pulmonary epithelium in 125 chronic smokers enrolled in a large, prospective
lung cancer chemoprevention study.
The status of two crucial tumor-suppressing genes, p16
and FHIT, were analyzed. Both are known to be damaged or silenced very early in
the process of cancer development. "There is substantial damage long before
there is cancer," Mao said.
Study participants gave both an oral and lung sample
initially and then again at three months. The researchers tracked whether either
p16, FHIT or both had been silenced by methylation. Patterns of methylation were
compared between the tissues.
The baseline tissue comparison showed methylation of
p16 in the lungs of 23 percent of study participants, of FHIT in 17 percent and
of either of the two genes in 35 percent. The percentages were similar in oral
tissue, with p16 methylated in 19 percent, FHIT in 15 percent and one of the two
in 31 percent.
Strong correlations were observed between methylation
patterns in both tissues. When methylation of either gene was considered positive,
37 of 39 individuals (95 percent) with p16 and/or FHIT promoter methylation in
the oral samples had promoter methylation in at least one matched bronchial sample.
This compared with only 59 of the 86 (69 percent) individuals without promoter
methylation in the oral samples. Similar correlations were seen at the three-month
analysis.
"Our study provides the first systematic evidence
that accessible tissue, the oral epithelium, can be used to monitor molecular
events in less accessible tissue," Bhutani said. "This provides a convenient
biomonitoring method to provide insight into the molecular events that take place
in the lungs of chronic smokers."
One follow-up area of study is to find additional biomarkers
in oral tissue. "We hope that our findings encourage researchers to test
an increasing compendium of biomarkers to confirm the reliability of oral epithelium
not only in lung cancer chemoprevention but also in therapeutic settings"
said Ashutosh Kumar Pathak, MD, another key study author and a post-doctoral fellow
in Surgical Oncology.
"Our study opens the door to enhancing our ability
to predict who has higher probability of getting tobacco-related cancers,"
Mao said. "Not only lung cancer, but pancreatic, bladder and head-and-neck
cancers, which also are associated with tobacco use."
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