2021 Fiscal Year Final Research Report
Molecular mechanisms of development and progression of non-TRU type lung adenocarcinoma.
Project/Area Number |
19K07441
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Review Section |
Basic Section 49020:Human pathology-related
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Research Institution | University of Tsukuba (2021) Jichi Medical University (2019-2020) |
Principal Investigator |
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Project Period (FY) |
2019-04-01 – 2022-03-31
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Keywords | non-TRU type / lung adenocarcinoma / TFF-1 / TTF-1 / HNF4alpha |
Outline of Final Research Achievements |
Molecular targeting of Non-TRU type lung adenocarcinomas is still an open field. We focused on TFF-1, which was characteristically highly expressed in non-TRU type cell lines. We reported that TFF-1 is highly expressed in non-TRU type adenocarcinomas, especially in gastrointestinal epithelial type adenocarcinomas that express high levels of HNF4α, and is involved in apoptosis inhibition and Anoikis resistance, making it a potential therapeutic target (Matsubara, 2020, Cancer Sci). We also elucidated the mechanism by which CADM1 acts in a tumour suppressive manner via the Hippo pathway in lung adenocarcinoma (Ito, Matsubara. 2019, Cancer Sci).
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Free Research Field |
肺癌病理
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Academic Significance and Societal Importance of the Research Achievements |
TRU-typeの肺腺癌では、EGFR変異、ALK転座、ROS1転座など、様々な分子標的が明らかとなり、予後の改善に貢献しているが、一方で、Non-TRU typeの肺腺癌においては、分子標的は定まっていない。Non-TRU typeの肺腺癌の中でも、胃型の性質を有するMucinous adenocarcinomaは、経気腔的に肺内転移を形成し、Stage I症例においても、極めて予後不良である。我々は、Mucinous adenocarcinomaなどのnon-TRU typeの悪性形質に関わる分子として、Anoikis抵抗性を促すTFF-1を見出し、新たな分子標的となりうることを示した。
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