STMN1 accumulation is associated with dysplastic and neoplastic lesions in patients with ulcerative colitis
Autor: | Takashi Yao, Hitoshi Ojima, Ken Shirabe, Reina Yajima, Takahiro Takada, Takehiko Yokobori, Ryo Takahashi, Hiroyuki Kuwano, Ryuji Kato, Katsuya Osone, Hiroomi Ogawa, Junichi Nakamura, Chika Katayama, Takaaki Fujii, Yoko Motegi, Hironori Tatsuski |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Cancer Research medicine.medical_specialty Colorectal cancer medicine.disease_cause Gastroenterology Inflammatory bowel disease colitic cancer 03 medical and health sciences 0302 clinical medicine dysplasia inflammatory bowel disease Internal medicine medicine Clinical significance ulcerative colitis business.industry Cancer Articles medicine.disease Ulcerative colitis 030104 developmental biology Oncology Dysplasia 030220 oncology & carcinogenesis Biomarker (medicine) business Carcinogenesis carcinogenesis |
Zdroj: | Oncology Letters |
ISSN: | 1792-1082 1792-1074 |
Popis: | Ulcerative colitis (UC) is thought to be associated with precancerous lesions that can ultimately lead to colon cancer. Therefore, diagnostic markers for colorectal dysplasia and cancer are urgently needed for patients with UC. Stathmin 1 (STMN1) is a novel cancer biomarker that is also a novel target for treatment in several cancers, including colon cancer. However, few studies have investigated the relationship between STMN1 expression and clinical features in colorectal dysplasia and cancer in patients with UC. The present study examined the clinical significance of STMN1 expression in colorectal dysplasia and cancer with UC. The present study performed an immunohistochemical analysis of 31 clinical colorectal samples from eight patients with colorectal dysplasia and/or cancer to assess the relationships between STMN1 expression and clinicopathological features including mismatch repair protein expression, rate of Ki-67 positivity, differentiation level, TNM stage, and UC duration. STNM1 expression was detected in 95.7% of dysplastic and cancerous lesions, whereas p53, the current diagnostic marker, was not expressed in 39.1% of dysplastic and cancerous lesions. Furthermore, STMN1 expression was associated with a high rate of positivity for Ki-67, a proliferation marker. Our data suggest that STMN1 in the colonic mucosa of UC patients may be useful as an early diagnostic marker of dysplasia and colitic cancer. |
Databáze: | OpenAIRE |
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