miR‑100‑5p and miR‑203a‑3p suppress esophageal squamous cell carcinoma progression by targeting FKBP5 Article Swipe
Hiroto Tanaka
,
Suguru Maruyama
,
Katsutoshi Shoda
,
Yoshihiko Kawaguchi
,
Yudai Higuchi
,
Takaomi Ozawa
,
Toshimitsu Nakayama
,
Ryo� Saito
,
Wataru Izumo
,
Koichi Takiguchi
,
Kensuke Shiraishi
,
Shinji Furuya
,
Hidetake Amemiya
,
Hiromichi Kawaida
,
Daisuke Ichikawa
·
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.3892/or.2025.9003
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.3892/or.2025.9003
Poorly differentiated cancers, including esophageal squamous cell carcinoma (ESCC), exhibit higher malignant potential and worse prognoses than well‑differentiated types. The present study aimed to identify microRNAs (miRNAs or miRs) involved in ESCC progression and their target mRNAs, focusing on tumor differentiation. miRNA candidates were selected using a miRNA array‑based approach and GEO datasets, comparing expression levels between poorly and non‑poorly differentiated ESCC. Clinical samples (n=61) and cell lines were analyzed to determine the significance and function of the selected miRNAs and their target mRNA. miR‑100‑5p and miR‑203a‑3p were significantly downregulated in poorly differentiated ESCC, with lower expression strongly associated with poorer overall survival (OS) (miR‑100‑5p: P=0.02; miR‑203a‑3p: P=0.05) and relapse‑free survival (RFS) (miR‑100‑5p: P=0.04; miR‑203a‑3p: P=0.12). Overexpression of these miRNAs suppressed cell migration and invasion. FKBP5 was identified as a common target, with its expression significantly reduced upon double‑transfection with miR‑100‑5p and miR‑203a‑3p. FKBP5 downregulation reduced tumor aggressiveness in KYSE70 cells, and clinical samples showed significantly worse survival rates in patients with high FKBP5 expression (OS: P=0.02; RFS: P=0.04). These findings suggest that miR‑100‑5p and miR‑203a‑3p act as tumor suppressors by targeting FKBP5, highlighting FKBP5 as a potential therapeutic target in ESCC.
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Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.3892/or.2025.9003
- http://www.spandidos-publications.com/10.3892/or.2025.9003/download
- OA Status
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- OpenAlex ID
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All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4414779442Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.3892/or.2025.9003Digital Object Identifier
- Title
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miR‑100‑5p and miR‑203a‑3p suppress esophageal squamous cell carcinoma progression by targeting FKBP5Work title
- Type
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articleOpenAlex work type
- Language
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enPrimary language
- Publication year
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2025Year of publication
- Publication date
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2025-10-03Full publication date if available
- Authors
-
Hiroto Tanaka, Suguru Maruyama, Katsutoshi Shoda, Yoshihiko Kawaguchi, Yudai Higuchi, Takaomi Ozawa, Toshimitsu Nakayama, Ryo� Saito, Wataru Izumo, Koichi Takiguchi, Kensuke Shiraishi, Shinji Furuya, Hidetake Amemiya, Hiromichi Kawaida, Daisuke IchikawaList of authors in order
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https://doi.org/10.3892/or.2025.9003Publisher landing page
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https://www.spandidos-publications.com/10.3892/or.2025.9003/downloadDirect link to full text PDF
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YesWhether a free full text is available
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hybridOpen access status per OpenAlex
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https://www.spandidos-publications.com/10.3892/or.2025.9003/downloadDirect OA link when available
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0Total citation count in OpenAlex
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| abstract_inverted_index.miR‑203a‑3p | 86, 175 |
| abstract_inverted_index.(miR‑100‑5p: | 104, 112 |
| abstract_inverted_index.differentiation. | 40 |
| abstract_inverted_index.miR‑203a‑3p. | 142 |
| abstract_inverted_index.miR‑203a‑3p: | 106, 114 |
| abstract_inverted_index.double‑transfection | 138 |
| abstract_inverted_index.well‑differentiated | 17 |
| cited_by_percentile_year | |
| countries_distinct_count | 1 |
| institutions_distinct_count | 15 |
| citation_normalized_percentile.value | 0.45364458 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | False |