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Hsa-miR-6743-5p Expression Varies with Lymph Node Metastasis in Esophageal Cancer.
- Source :
-
Clinical laboratory [Clin Lab] 2018 Jul 01; Vol. 64 (7), pp. 1249-1257. - Publication Year :
- 2018
-
Abstract
- Background: Recently, esophageal cancer has become more common in China. To find a molecular biomarker will provide a handy way to improve precancerous diagnosis and evaluate the state of lymph node metastasis, improving prognosis. The present study aimed to investigate the expression level of hsa-miR-6743-5p in 25 esophageal tissues and to estimate the correlation between clinicopathological features of esophageal squamous cell cancer with miR-6743-5p expression.<br />Methods: Quantitative reverse transcription polymerase chain reaction was performed to examine the expression level of miR-6743-5p in 25 pairs of esophageal cancer tissues and adjacent non-cancerous tissues. The correlation between miR-6743-5p level and clinical characteristics was determined.<br />Results: The examined esophageal squamous cell cancer tissues exhibited no statistical difference on miR-6743-5p expression compared to the adjacent non-tumor tissues. miR-6743-5p was positively associated with lymph node metastasis. Downregulation of miR-6743-5p was found in the patients with lymph node metastasis while upregulation of miR-6743-5p was found in those without lymph node metastasis.<br />Conclusions: Our study suggests that the expression of miR-6743-5p is different in different lymph node metastasis statuses. miR-6743-5p expression is downregulated in patients with lymph node metastasis in esophageal cancer.
- Subjects :
- Aged
Asian People genetics
Biomarkers, Tumor genetics
Carcinoma, Squamous Cell ethnology
Carcinoma, Squamous Cell pathology
China
Down-Regulation
Esophageal Neoplasms ethnology
Esophageal Neoplasms pathology
Female
Humans
Lymphatic Metastasis
Male
Middle Aged
Prognosis
Carcinoma, Squamous Cell genetics
Esophageal Neoplasms genetics
Gene Expression Regulation, Neoplastic
MicroRNAs genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1433-6510
- Volume :
- 64
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Clinical laboratory
- Publication Type :
- Academic Journal
- Accession number :
- 30146847
- Full Text :
- https://doi.org/10.7754/Clin.Lab.2018.180314