Pulmonary adenocarcinoma in situ

Seijiro Sato, Noriko Motoi, Miyako Hiramatsu, Eisaku Miyauchi, Hiroshi Ono, Yuichi Saito, Hiroko Nagano, Hironori Ninomiya, Kentaro Inamura, Hirofumi Uehara, Mingyon Mun, Yukinori Sakao, Sakae Okumura, Masanori Tsuchida, Yuichi Ishikawa

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

Lung adenocarcinomas in situ (AISs) often occur in individuals who have never smoked, although smoking is one of the main causes of lung cancer. To characterize AIS and, in particular, determine how AIS might be related to smoking, we collected a large number of AIS cases and examined clinicopathologic features, EGFR and KRAS mutation status, and activation status of receptor tyrosine kinase downstream signal pathways, including pAkt, pERK, and pStat3, using immunohistochemistry. We identified 110 AISs (36 smokers and 74 nonsmokers) among 1549 adenocarcinomas resected surgically during 1995 to 2010. Between the AIS of smokers and nonsmokers, only the sex ratio was significantly different; all the other clinicopathologic factors including TTF-1 and driver mutations were not significantly different: EGFR and KRAS mutation rates (smokers:nonsmokers) were 61:58 (%) (P=0.7) and 6.1:1.4 (%) (P=0.2), respectively, whereas, in invasive adenocarcinomas, the rates were 41:69 (%) (P<0.001) and 9.4:2.3 (%) (P<0.04), respectively. For pAkt and pERK, around 40% to 50% of AISs were positive, and for pStat3, >80% were positive, with no significant differences between smokers and nonsmokers with AIS. Mucinous AIS (n=8) rarely harbored KRAS mutations and expressed significantly less pStat3 (P<0.001) than nonmucinous AIS. Taken together, AIS occurs predominantly in female individuals and nonsmokers. However, characteristics of AIS arising in smokers and nonsmokers were similar in terms of cell lineage, driver mutations, and receptor tyrosine kinase pathway activation. Our results suggest that smoking is not a major cause of AIS. Rather, smoking may play a role in progression of AIS to invasive adenocarcinoma with AIS features.

Original languageEnglish
Pages (from-to)912-921
Number of pages10
JournalAmerican Journal of Surgical Pathology
Volume39
Issue number7
DOIs
Publication statusPublished - 2015 Jun 29
Externally publishedYes

Keywords

  • adenocarcinoma in situ (AIS)
  • driver mutations
  • lung
  • receptor tyrosine kinase pathway
  • smoking

ASJC Scopus subject areas

  • Anatomy
  • Surgery
  • Pathology and Forensic Medicine

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