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Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer.
Oh, Hyunseung; Kim, Soon Gu; Bae, Sung Uk; Byun, Sang Jun; Kim, Shin; Lee, Jae-Ho; Hwang, Ilseon; Kwon, Sun Young; Lee, Hye Won.
Afiliación
  • Oh H; Department of Pathology, Keimyung University School of Medicine, Daegu, Korea.
  • Kim SG; Department of Education Support Center, Keimyung University School of Medicine, Daegu, Korea.
  • Bae SU; Division of Colorectal Surgery, Department of Surgery, Keimyung University School of Medicine, Daegu, Korea.
  • Byun SJ; Department of Radiation Oncology, Keimyung University School of Medicine, Daegu, Korea.
  • Kim S; Department of Immunology, Keimyung University School of Medicine, Daegu, Korea.
  • Lee JH; Department of Anatomy, Keimyung University School of Medicine, Daegu, Korea.
  • Hwang I; Department of Pathology, Keimyung University School of Medicine, Daegu, Korea.
  • Kwon SY; Department of Pathology, Keimyung University School of Medicine, Daegu, Korea.
  • Lee HW; Department of Pathology, Keimyung University School of Medicine, Daegu, Korea.
J Pathol Transl Med ; 56(1): 40-47, 2022 Jan.
Article en En | MEDLINE | ID: mdl-34775733
BACKGROUND: Polo-like kinase 4 (PLK4) is a serine/threonine protein kinase located in the centriole of the chromosome during the cell cycle. PLK4 overexpression has been described in a variety of many common human epithelial tumors. Conversely, PLK4 acts as a haploinsufficient tumor suppressor in some situations, highlighting the importance of strict regulation of PLK4 expression, activity, and function. Meanwhile, the importance of chemoradiation resistance in rectal cancer is being emphasized more than ever. We aimed to analyze PLK4 expression and the tumor regression grade (TRG) in patients with rectal cancer, treated with chemoradiotherapy (CRT). METHODS: A retrospective study was conducted on 102 patients with rectal cancer who received preoperative CRT. Immunohistochemistry for PLK4 in paraffin-embedded tissue was performed from the biopsy and surgical specimens. RESULTS: We found significant association between high expression of PLK4 and poor response to neoadjuvant CRT (according to both Mandard and The Korean Society of Pathologists TRG systems) in the pre-CRT specimens. Other clinicopathologic parameters did not reveal any correlation with PLK4 expression. CONCLUSIONS: This study revealed an association between high expression of PLK4 in the pre-CRT specimens and TRG. Our results indicated that PLK4 could potentially be a new predictor for CRT effect in patients with rectal cancer.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Pathol Transl Med Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Pathol Transl Med Año: 2022 Tipo del documento: Article