Evidence map›Paper›PMID 26993826›Full record

ArticleDigestive diseases and sciences2016

CHST11/13 Regulate the Metastasis and Chemosensitivity of Human Hepatocellular Carcinoma Cells Via Mitogen-Activated Protein Kinase Pathway.

Huimin Zhou, Yanping Li, Xiaobo Song, Yongfu Zhao, Lei Cheng, Lifen Zhao, Li Jia

Abstract read
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In one paragraph

Article in Digestive diseases and sciences, 2016. 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 22% 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, 31 citations in OpenAlex.

  1. Review
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  9. Using Transcriptional Signatures to Find Cancer Drivers with LURE.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2020
    Article
  10. Inhibition of protein FAK enhances 5-FU chemosensitivity to gastric carcinomaComputational and structural biotechnology journal · 2020
    Article
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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 at 2 institutions in 2 countries.

Huimin ZhouCollege of Laboratory Medicine, Dalian Medical University, 9 Lvshunnan Road Xiduan, Dalian, 116044, Liaoning Province, China.
Yanping LiCollege of Laboratory Medicine, Dalian Medical University, 9 Lvshunnan Road Xiduan, Dalian, 116044, Liaoning Province, China.
Xiaobo SongDepartment of Medical Biology, Faculty of Health Sciences, University of Tromsø, 9037, Tromsö, Norway.
Yongfu ZhaoDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian, 116027, Liaoning Province, China.
Lei ChengDepartment of Laparoscopic Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, Liaoning Province, China.
Lifen ZhaoCollege of Laboratory Medicine, Dalian Medical University, 9 Lvshunnan Road Xiduan, Dalian, 116044, Liaoning Province, China.
Li JiaCollege of Laboratory Medicine, Dalian Medical University, 9 Lvshunnan Road Xiduan, Dalian, 116044, Liaoning Province, China. jiali0386@sina.com.ORCID 0000-0003-3152-3253
Dalian Medical University · CNUiT The Arctic University of Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarbohydrate sulfotransferases 11-13 (CHST11-13), that catalyze the transfer of sulfate to position 4 of the GalNAc residue of chondroitin, have been implicated in various diseases.

aimThis study aimed to clarify the association of CHST11-13 expression with metastasis and drug sensitivity in hepatocellular carcinoma (HCC) cells.

methodsWe measured the levels of CHST11 and CHST13 in a series of HCC cells using real-time PCR and Western blotting. After RNAi and forced expression treatment of CHST11 and CHST13 in MHCC97L and MHCC97H cells, metastatic potential and drug sensitivity of the two cells were investigated with ECM invasion assay, drug sensitivity assay, and in vivo antitumor activity assay. By real-time PCR and Western blotting, we explored the possible impacts of these two genes on mitogen-activated protein kinase (MAPK) signal pathway. MAPK pathway was blocked by PD98059 or SP600125 to elucidate the effects of MAPK pathway on metastasis and chemosensitivity.

resultsSignificantly reduced levels of CHST11 and CHST13 were observed in highly invasive MHCC97H cells compared with those of MHCC97L cell line with low metastatic potential. Decreased or forced expression of CHST11 and CHST13 altered metastatic potential and drug sensitivity of MHCC97L and MHCC97H cells. Remarkable alteration of MAPK activity was shown in two HCC cells with genetic manipulation. Conversely, pharmacologic inhibition of the MAPK pathway suppressed invasive potential and rescued drug sensitivity of MHCC97H cells.

conclusionsOur results have demonstrated that CHST11 and CHST13 negatively modulate metastasis and drug resistance of HCC cells probably via oncogenic MAPK signal pathway.

Indexed as

Carcinoma, HepatocellularCell Line, TumorFemaleGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansLiver NeoplasmsMaleMAP Kinase Signaling SystemMiddle AgedNeoplasm MetastasisRNA, Small InterferingSulfotransferasesCHST11 protein, humanCHST12 protein, humanCHST13 protein, humanRNA, Small InterferingSulfotransferasesCarbohydrate sulfotransferaseDrug sensitivityHuman hepatocellular carcinomaMAPK signaling pathwayMetastasis

Identifiers

PMID26993826
OpenAlexW2298345106

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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.