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pmid:32196963

miR-143 inhibits renal cell carcinoma cells metastatic potential by suppressing ABL2.

Bin Xu · Can Wang · Ya-Li Wang · Shu-Qiu Chen · Jian-Ping Wu · Wei-Dong Zhu · Chun-Ying Wang · Han Guan · Chao Guan · Zong-Hao You · Ming Chen

The Kaohsiung journal of medical sciences · 2020 doi:10.1002/kjm2.12207

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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miR-143 inhibits renal cell carcinoma cells metastatic potential by suppressing ABL2.
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10.1002/kjm2.12207
pmid
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Bin Xu
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Can Wang
[2]
Ya-Li Wang
[3]
Shu-Qiu Chen
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Jian-Ping Wu
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Wei-Dong Zhu
[6]
Chun-Ying Wang
[7]
Han Guan
[8]
Chao Guan
[9]
Zong-Hao You
[10]
Ming Chen
journal
The Kaohsiung journal of medical sciences
year
2020
abstract
Although micro RNA (miRNA) expression profiles are widely investigated in renal cell carcinoma (RCC), their potential roles for affecting RCC initiation and progression remain largely unknown. Here, we examined the aberrant expression profiles of miRNAs inhuman metastatic RCC tissues based on Gene Expression Omnibus (GSE37989). We further validated them iRNAs expression data in the largest clinical dataset: The Cancer Genome Atlas (TCGA). And cell adhesion and migration abilities and epithelial me senchymal transition (EMT) related proteins were assessed in both normal and tumor RCC cell lines. We suggest that hsa-miR-143 is a potential tumor suppressor in RCC as its down regulation positively correlated with adverse prognosis. Biologically, cell adhesion, migration, and EMT were dramatically inhibited by miR-143. Mechanistically, we found that miR-143 targets ABL proto-oncogene 2 (ABL2), which was also found to be an indicator for poor survival in TCGA database. Our results have important implications in understanding functions of miRNAs in metastatic RCC and will provide a basis for further clinical application.
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Identification of metastamirs as metastasis-associated microRNAs in clear cell renal cell carcinomas
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MATERIALS AND METHODS Cell culture and transfection 786‐O which is a human RCC cell line with me
[1]
d with 10% FBS. 786‐O cells were transiently transfected with miR‐143 and negative control (NC) mimic
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Sciences (Shanghai, China). HK‐2 cells were cultured in Dulbecco's modified Eagle's medium (DMEM) wi
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etal bovine serum (FBS) and 786‐O cells were cultured in RPMI 1640 supplemented with 10% FBS. 786‐O c
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Cells were seeded in 6‐well plates and transfected with 5 nM of miR‐143 mimics or NC mimics. Cl"], "order_basis": "paper_text_order:1218", "id": "assay:1"}, {"role": "data_generation", "definition_id": "cell_culture", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["Sciences (Shanghai, China). HK‐2 cells were cultured in Dulbecco's modified Eagle's medium (DMEM) wi", "etal bovine serum (FBS) and 786‐O cells were cultured in RPMI 1640 supplemented with 10% FBS. 786‐O c"], "order_basis": "paper_text_order:1474", "id": "assay:2"}, {"role": "analysis", "definition_id": "group_comparison", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["The significance of differences between groups was estimated by Student's t test. Overall survival rates were calculated by the Kaplan‐Meier method with the log‐rank test applied for comparison."], "order_basis": "consumes_earlier_output", "id": "assay:3"}]}