Comparison of Akt/mammalian target of rapamycin/4E-binding protein 1 pathway signal activation in round stromal and surface cells in patients with sclerosing pneumocytoma

• Published in: Pathology, research and practice research and practice, 2023-04, Vol.244, p.154384-154384, Article 154384
• Main Authors: Hashisako, Mikiko, Iwasaki, Takeshi, Matsumoto, Takamasa, Yamada, Yuichi, Miyamoto, Takumi, Taniguchi, Midori, Oishi, Chiemi, Oda, Yoshinao
• Format: Article
• Language: English
• Subjects: Akt/mTOR/4EBP1 pathway; AKT1; Humans; Lung Neoplasms - genetics; Lung Neoplasms - pathology; Proto-Oncogene Proteins c-akt - metabolism; Round cell; Sclerosing pneumocytoma; Signal Transduction; Sirolimus; Surface cell; TOR Serine-Threonine Kinases - metabolism
• ISSN: 0344-0338; 1618-0631
• DOI: 10.1016/j.prp.2023.154384

Sclerosing pneumocytoma (SP) is a rare benign epithelial tumor of the lung, and approximately 40 % of patients with SP present with AKT1 E17K mutation. SP cells comprise proliferated surface and round stromal cells. To elucidate the role of signal transductions and to identify the difference between surface and stromal cells, the current study aimed to investigate the activation of the Akt/mammalian target of rapamycin (mTOR)/4E-binding protein 1 signaling pathway in SP. The molecular and pathological characteristics of SP in 12 patients were analyzed. AKT1 gene analysis revealed AKT1 E17K mutation in four cases. Immunohistochemical analysis revealed that tumor cells were cytoplasmic positive for pAkt, pmTOR, p4EBP1, and pS6RP. The surface cells had a significantly higher expression of pmTOR (p = 0.002) and a significantly lower expression of p4EBP1 (p = 0.017) than stromal cells. SP without AKT1 E17K mutation had a higher positive correlation with pacts, p4EBP1, pmTOR, and pS6RP expression than SP with AKT1 E17K mutation. These findings may be attributed to the aberrant activation of the Akt/mTOR pathway due to AKT1 E17K mutations. Hence, both surface and round stromal cells have tumorigenic characteristics, and differences in these characteristics may contribute to variations in tumor growth and the morphology and angiogenesis of SP.