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  1. 学内発行雑誌
  2. The Showa University journal of medical sciences
  3. Vol.33(2021)
  4. No.2

Clinicopathological study on pIgR expression and tumor progression in advanced colorectal cancer

https://showa.repo.nii.ac.jp/records/3811
https://showa.repo.nii.ac.jp/records/3811
a719455c-15b6-4746-81cd-2698a4b9eba2
名前 / ファイル ライセンス アクション
S33_41.pdf S33_41.pdf (287.8 kB)
Item type 学内発行雑誌 / Departmental Bulletin Paper(1)
公開日 2021-07-28
タイトル
タイトル Clinicopathological study on pIgR expression and tumor progression in advanced colorectal cancer
言語 en
言語
言語 eng
資源タイプ
資源タイプ departmental bulletin paper
著者 KIKUCHI, Kazuo

× KIKUCHI, Kazuo

KIKUCHI, Kazuo

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OHIKE, Nobuyuki

× OHIKE, Nobuyuki

OHIKE, Nobuyuki

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NOROSE, Tomoko

× NOROSE, Tomoko

NOROSE, Tomoko

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YOSHIDA, Hitoshi

× YOSHIDA, Hitoshi

YOSHIDA, Hitoshi

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OGAWA, Takashi

× OGAWA, Takashi

OGAWA, Takashi

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YAMOCHI, Toshiko

× YAMOCHI, Toshiko

YAMOCHI, Toshiko

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書誌情報 The Showa University journal of medical sciences

巻 33, 号 2, p. 41-46, 発行日 2021-06
抄録
内容記述タイプ Abstract
内容記述 This study is aimed at investigating the relationship between the polymeric immunoglobulin receptor (pIgR) expression and clinicopathological factors in advanced colorectal cancer (CRC) patients. The study involved 47 advanced CRC patients who were surgically resected and underwent KRAS gene test. The pIgR expression was analyzed by immunohistochemistry, and the patients were classified into high and low (pIgR-H and pIgR-L, respectively) groups based on the staining intensity and range. A total of 13 cases was classified under the pIgR-H group, and the remaining 34 were classified under the pIgR-L group. Results suggest no significant differences in most clinicopathological factors between the pIgR-H and pIgR-L groups, although the pIgR-L group had a significantly higher frequency of venous invasion than the pIgR-H group, whereas the frequency of KRAS gene mutation was significantly higher in the pIgR-H group than that in the pIgR-L group. The findings in this study showed little significant correlation between the pIgR expression and clinicopathological factors in advanced CRC patients. Further research on the biological behavior of pIgR as a drug treatment option for KRAS-mutated advanced CRCs is also warranted.
DOI
関連タイプ isIdenticalTo
関連識別子 10.15369/sujms.33.41
出版者
出版者 Showa University Society
ISSN
収録物識別子タイプ ISSN
収録物識別子 2185-0968
出版タイプ
出版タイプ VoR
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