Evidence map›Paper›PMID 33236127›Full record

ArticleMolecular medicine reports2021

Exosomal‑miR‑10a derived from colorectal cancer cells suppresses migration of human lung fibroblasts, and expression of IL‑6, IL‑8 and IL‑1β.

Jian Wang, Yuanting Liu, Ying Li, Xuan Zheng, Jianhui Gan, Zhaoyuan Wan, Jun Zhang, Yan Liu, Yaqi Wang, Wanning Hu and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

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  9. Exploring the interplay betweenFrontiers in microbiology · 2023
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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

12 authors at 1 institution in 1 country.

Jian Wang *Department of Gastrointestinal Surgery, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Yuanting Liu *Department of Gastrointestinal Surgery, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Ying LiNuclear Medicine Clinical Laboratory, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Xuan ZhengNuclear Medicine Clinical Laboratory, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Jianhui GanDepartment of Anesthesiology, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Zhaoyuan WanThe Cancer Institute, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Jun ZhangThe Cancer Institute, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Yan LiuThe Cancer Institute, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Yaqi WangDepartment of Breast Surgery, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Wanning HuThe Cancer Institute, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Yufeng LiThe Cancer Institute, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Yankun LiuThe Cancer Institute, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Tangshan People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRs) carried in exosomes serve an important role in the pre‑metastatic microenvironment and in intercellular interactions. However, the function of exosomal‑miR‑10a derived from primary colorectal cancer (CRC) cells on fibroblasts in the lung metastatic microenvironment of patients with CRC remains unclear. Reverse transcription‑quantitative PCR was performed using samples from patients with CRC, and demonstrated that the expression levels of miR‑10a were significantly lower in serum and cancer tissue samples from patients with CRC compared with in serum from healthy individuals and paired non‑cancerous tissues, respectively. In addition, the expression levels of miR‑10a were inversely associated with the invasion depth of CRC. Exosomal‑miR‑10a derived from CRC cells reduced the proliferative and migratory activities of primary normal human lung fibroblasts (NHLFs), and the expression levels of IL‑6, IL‑8 and IL‑1β in NHLFs. The present study provided insight into the phenotypic alterations of NHLFs induced by exosomal‑miR‑10a derived from CRC cells, which may aid understanding of the mechanism underlying the process of CRC lung metastasis.

Indexed as

Cell MovementGene Expression Regulation, NeoplasticCell Line, TumorCoculture TechniquesColorectal NeoplasmsExosomesFibroblastsHumansInterleukin-1betaInterleukin-6Interleukin-8LungMicroRNAsNeoplasm ProteinsRNA, NeoplasmCXCL8 protein, humanIL1B protein, humanIL6 protein, humanInterleukin-1betaInterleukin-6Interleukin-8MicroRNAsMIRN10 microRNA, humanNeoplasm ProteinsRNA, Neoplasmcolorectal cancerexosomelung fibroblastsmicroenvironmentmicroRNA‑10a

Identifiers

PMID33236127
PMCPMC7716406
OpenAlexW3109017315

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.