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pmid:32184614

Hsa_circ_103973 Acts as a Sponge of miR-335 to Promote Cervical Cancer Progression.

Yingping Zhu · Xuelu Jiang · Shuo Zhang · Lingcong Wang · Qun Zhou · Jun Jiang

OncoTargets and therapy · 2020 doi:10.2147/OTT.S215736

Paper

complete

Experiment

complete

Data

partial

Analysis

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absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Hsa_circ_103973 Acts as a Sponge of miR-335 to Promote Cervical Cancer Progression.
doi
10.2147/OTT.S215736
pmid
32184614
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[0]
Yingping Zhu
[1]
Xuelu Jiang
[2]
Shuo Zhang
[3]
Lingcong Wang
[4]
Qun Zhou
[5]
Jun Jiang
journal
OncoTargets and therapy
year
2020
abstract
BACKGROUND: Cervical cancer (CC) ranks as the second most common malignancy in women, accounting for more two 2 million deaths every year in the world. Recently, circular RNAs (circRNAs) have been reported to regulate the progression of multiple human tumors; however, whether it involves in CC remains largely elusive. MATERIALS AND METHODS: Two GEO circRNA expression profiles (GSE102686, GSE113696) were downloaded to analyze the differentially expressed circRNAs using bioinformatics methods. Expression of circ_103973, miR-335 and PPP6C in CC tissues and cell lines were examined by qRT-PCR. Cell apoptosis was assessed with PI/Annexin-V double staining followed by the analysis of flow cytometry. Cell proliferation was evaluated by MTT and colony formation assays. Interaction between circ_103973 and miR-335, as well as miR-335 and PPP6C, were verified by dual-luciferase reporter assay. RESULTS: Circ_103973 was found to be highly expressed in both GSE102686 and GSE113696 datasets as well as in CC tissue samples and cell lines. Higher levels of circ_103973 were correlated to a worse outcome of CC patients. Knockdown of circ_103973 significantly promoted CC cell apoptosis and inhibited CC cell proliferation in vitro. Mechanistically, we demonstrated that circ_103973 served as a sponge of miR-335, which directly targeted PPP6C in CC cells. miR-335 was found to be decreased in CC, while PPP6C was found to be increased in CC. Moreover, anti-miR-335 could reverse the inhibitory effects of circ_103973 knockdown on CC cell proliferation, and this phenomenon could be blocked by si-PPP6C. CONCLUSION: Circ_103973 promoted CC cell proliferation in vitro by physically binding miR-335, which further targeted and regulated PPP6C.
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Circular RNA profile of human cervical squamous cell carcinoma
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Primer Sequences Used In This Study
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nd cell lines were examined by qRT-PCR. Cell apoptosis was assessed with PI/Annexin-V double staini
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f circ_103973 significantly promoted CC cell apoptosis and inhibited CC cell proliferation in vitro
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double staining followed by the analysis of flow cytometry. Cell proliferation was evaluated by MTT and
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orrelated to a worse outcome of CC patients. Knockdown of circ_103973 significantly promoted CC cel
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everse the inhibitory effects of circ_103973 knockdown on CC cell proliferation, and this phenomeno
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Complete file
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Recently, circular RNAs (circRNAs) have been reported to regulate the progression of multiple human tumors; however, whether it involves in CC remains largely elusive.\nMATERIALS AND METHODS: Two GEO circRNA expression profiles (GSE102686, GSE113696) were downloaded to analyze the differentially expressed circRNAs using bioinformatics methods. Expression of circ_103973, miR-335 and PPP6C in CC tissues and cell lines were examined by qRT-PCR. Cell apoptosis was assessed with PI/Annexin-V double staining followed by the analysis of flow cytometry. Cell proliferation was evaluated by MTT and colony formation assays. Interaction between circ_103973 and miR-335, as well as miR-335 and PPP6C, were verified by dual-luciferase reporter assay.\nRESULTS: Circ_103973 was found to be highly expressed in both GSE102686 and GSE113696 datasets as well as in CC tissue samples and cell lines. Higher levels of circ_103973 were correlated to a worse outcome of CC patients. Knockdown of circ_103973 significantly promoted CC cell apoptosis and inhibited CC cell proliferation in vitro. Mechanistically, we demonstrated that circ_103973 served as a sponge of miR-335, which directly targeted PPP6C in CC cells. miR-335 was found to be decreased in CC, while PPP6C was found to be increased in CC. Moreover, anti-miR-335 could reverse the inhibitory effects of circ_103973 knockdown on CC cell proliferation, and this phenomenon could be blocked by si-PPP6C.\nCONCLUSION: Circ_103973 promoted CC cell proliferation in vitro by physically binding miR-335, which further targeted and regulated PPP6C.", "claims": [{"id": "claim-method", "statement": "Statistical analysis was conducted on SPSS v20 software (IBM Corp., Armonk, NY, USA) using one-way analysis of variance.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32184614", "locator": "sections[13] \"Statistical Analysis\" paragraph 2", "quote": "Statistical analysis was conducted on SPSS v20 software (IBM Corp., Armonk, NY, USA) using one-way analysis of variance."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Two GEO circRNA expression profiles (GSE102686, GSE113696) were downloaded to analyze the differentially expressed circRNAs using bioinformatics methods.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32184614", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Two GEO circRNA expression profiles (GSE102686, GSE113696) were downloaded to analyze the differentially expressed circRNAs using bioinformatics methods."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:32184614"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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