Evidence map›Paper›PMID 26662310›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

miR-615-5p prevents proliferation and migration through negatively regulating serine hydromethyltransferase 2 (SHMT2) in hepatocellular carcinoma.

Xiaoyu Wu, Liang Deng, Decai Tang, Gang Ying, Xuequan Yao, Fukun Liu, Gui Liang

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

29 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. Frontiers in oncology · 2024
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  19. Reprogramming of serine, glycine and one-carbon metabolism in cancer.Biochimica et biophysica acta. Molecular basis of disease · 2020
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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

7 authors.

Xiaoyu WuDepartment of Surgical Oncology, Affiliated Hospital of Nanjing University of Traditional Chinese Medicine, 155 Hanzhong Road, Nanjing, 210029, China.
Liang DengDepartment of Hepatobiliary Surgery, the Eastern Hospital of the First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510700, China., Sun Yat-sen University, Guangzhou, 510700, People's Republic of China.
Decai TangNanjing University of Traditional Chinese Medicine, 282 Hanzhong Road, Nanjing, 210029, China.
Gang YingNanjing University of Traditional Chinese Medicine, 282 Hanzhong Road, Nanjing, 210029, China.
Xuequan YaoNanjing University of Traditional Chinese Medicine, 282 Hanzhong Road, Nanjing, 210029, China.
Fukun LiuNanjing University of Traditional Chinese Medicine, 282 Hanzhong Road, Nanjing, 210029, China.
Gui LiangDepartment of General Surgery, Jiangsu Cancer Hospital, The Affiliated Cancer Hospital of Nanjing Medical University, 42 Baiziting, Nanjing, 210009, China. gs_gliang@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been reported that miR-615-5p was upregulated in hepatocellular carcinoma (HCC) preventing both growth and migration. However, the underlying mechanism by which miR-615-5p played a role in HCC remains unknown. Here, in our present study, to investigate the mechanism of miR-615-5p, bioinformatic prediction and luciferase reporter assay were employed to ascertain the downstream target of miR-615-5p finding that the serine hydromethyltransferase 2 (SHMT2) was the direct downstream target. Knockdown or overexpression of miR-615-5p can lead to increasing or decreasing expression of SHMT2 in HCC cells. Besides, knockdown or overexpression of SHMT2 can suppress or promote both proliferation and migration of HCC cells, indicating that miR-615-5p can directly and negatively regulate the SHMT2 in HCC cells. In addition, to understand the clinicopathological significance of SHMT2 expression in HCC, immunohistochemistry was performed. It was found that SHMT2 expression was significantly associated with poor prognosis and TNM stage. Together, our results for the first time showed that miR-615-5p prevents proliferation and migration through negatively regulating SHMT2 in HCC.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedBase SequenceBinding SitesCarcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationFemaleGlycine HydroxymethyltransferaseHumansKaplan-Meier EstimateLiver NeoplasmsMaleMicroRNAsGlycine HydroxymethyltransferaseMicroRNAsMIRN615 microRNA, humanRNA, MessengerSHMT protein, humanHepatocellular carcinoma (HCC)MigrationmiR-615-5pProliferationSHMT2

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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.