Evidence map›Paper›PMID 33125087›Full record

ArticleInternational journal of molecular medicine2020

Hypoxia‑induced circCCDC66 promotes the tumorigenesis of colorectal cancer via the miR‑3140/autophagy pathway.

Jin Feng, Zhong Li, Ling Li, Haibin Xie, Qicheng Lu, Xiaozhou He

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

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  16. Circular RNA-regulated autophagy is involved in cancer progression.Frontiers in cell and developmental biology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Jin FengDepartment of Gastrointestinal Surgery, The First People's Hospital of Changzhou, Changzhou, Jiangsu 213029, P.R. China.
Zhong LiDepartment of Gastrointestinal Surgery, The First People's Hospital of Changzhou, Changzhou, Jiangsu 213029, P.R. China.
Ling LiDepartment of Gastrointestinal Surgery, The First People's Hospital of Changzhou, Changzhou, Jiangsu 213029, P.R. China.
Haibin XieDepartment of Gastrointestinal Surgery, The First People's Hospital of Changzhou, Changzhou, Jiangsu 213029, P.R. China.
Qicheng LuDepartment of Gastrointestinal Surgery, The First People's Hospital of Changzhou, Changzhou, Jiangsu 213029, P.R. China.
Xiaozhou HeDepartment of Urology Surgery, The First People's Hospital of Changzhou, Changzhou, Jiangsu 213029, P.R. China.
The First People's Hospital of Changzhou · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circular RNAs (circRNAs) have been reported to be involved in the progression of colorectal cancer (CRC). However, the biological role of circCCDC66 in CRC remains unclear. Therefore, the present study aimed to elucidate the mechanisms through which circCCDC66 affects the hypoxia‑induced progression of CRC. It was found that hypoxia promoted the progression of CRC and upregulated the expression of circCCDC66. Furthermore, circCCDC66‑knockdown reduced viability, migration and invasion, and enhanced the apoptosis of hypoxia‑exposed CRC cells. Using the starBase database, it was identified that circCCDC66 may bind to miR‑3140. Subsequently, it was confirmed that circCCDC66 serves as a sponge of miR‑3140 and the depletion of miR‑3140 partly abolished the effects of circCCDC66 on the phenotype of hypoxia‑exposed CRC cells. In addition, miR‑3140 was validated to inhibit the autophagy pathway. The use of an autophagy inducer partially reversed the miR‑3140 overexpression‑induced inhibition of the viability and invasion, and the promotion of the apoptosis of hypoxia‑exposed CRC cells. In summary, the findings of the present study demonstrated that circCCDC66 facilitates the development of CRC cells under hypoxic conditions via regulation of miR‑3140/autophagy. These findings may provide a novel therapeutic option for patients with CRC.

Indexed as

AdultAgedAutophagyBase SequenceCarcinogenesisCell HypoxiaCell Line, TumorColorectal NeoplasmsDisease ProgressionFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesGene SilencingHCT116 CellsHumansMaleMicroRNAsMIRN3140 microRNA, humanRNA, Circular

Identifiers

PMID33125087
PMCPMC7595663
OpenAlexW3091806379

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.