Evidence map›Paper›PMID 27235117›Full record

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

Silencing of ST6GalNAc I suppresses the proliferation, migration and invasion of hepatocarcinoma cells through PI3K/AKT/NF-κB pathway.

Xiao Yu, Qiang Wu, Liping Wang, Yujie Zhao, Qingqing Zhang, Qingtao Meng, Pawan, Shujing Wang

Erratum issuedAbstract read
PubMed Publisher
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. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Xiao YuDepartment of Pathology, Dalian Medical University, Dalian, 116044, Liaoning Province, China.
Qiang WuDepartment of Biochemistry and Molecular Biology, Institute of Glycobiology, Dalian Medical University, Lvshun South Road, Dalian, 116044, Liaoning Province, China.
Liping WangDepartment of Biochemistry and Molecular Biology, Institute of Glycobiology, Dalian Medical University, Lvshun South Road, Dalian, 116044, Liaoning Province, China.
Yujie ZhaoDepartment of Biochemistry and Molecular Biology, Institute of Glycobiology, Dalian Medical University, Lvshun South Road, Dalian, 116044, Liaoning Province, China.
Qingqing ZhangDepartment of Pathology, Dalian Medical University, Dalian, 116044, Liaoning Province, China.
Qingtao MengDepartment of Surgery, The Third People's Hospital of Dalian, Affiliated Hospital of Dalian Medical University, Dalian, 116000, Liaoning Province, China.
PawanDepartment of Pathology, Dalian Medical University, Dalian, 116044, Liaoning Province, China.
Shujing WangDepartment of Biochemistry and Molecular Biology, Institute of Glycobiology, Dalian Medical University, Lvshun South Road, Dalian, 116044, Liaoning Province, China. wangshujing@dlmedu.edu.cn.
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ST6GalNAc I is the major Sialyl-Tn antigen (STn) synthase that is highly correlated with tumor invasion and metastasis. However, the roles and molecular mechanisms by which ST6GalNAc I mediates the malignant phenotypes of hepatocarcinoma cells still remain poorly unknown. In this study, we investigated the expression of STn and ST6GalNAc I in mouse hepatocarcinoma cell lines Hca-F, Hca-P, and Hepa1-6, which have different metastatic potential, as compared with normal mouse liver cell line IAR-20. The results showed that the expression of ST6GalNAc I and STn in Hca-F and Hca-P cells was much higher than that in Hepa1-6 and IAR20 cells. Knockdown of ST6GalNAc I by shRNA in Hca-F cells significantly decreased the expression of STn and inhibited the growth of tumor cells in vitro and in vivo. This reduction of ST6GalNAc I expression also led to the decreased migration and invasion of Hca-F cells. Furthermore, we found that ST6GalNAc I knockdown inhibited the expression levels of PI3k, p-Akt473, p-Akt308, NF-κB, and their downstream molecules. Together, our results suggest a role of ST6GalNAc I in promoting the growth and invasion of hepatocarcinoma cells through regulating PI3K/AKT signaling, and ST6GalNAc I might be a promising marker for the prognosis and therapy of hepatocarcinoma.

Indexed as

RNA InterferenceAnimalsAntigens, Tumor-Associated, CarbohydrateBlotting, WesternCarcinoma, HepatocellularCell MovementCell ProliferationImmunohistochemistryLiver NeoplasmsMice, Inbred StrainsMicroscopy, FluorescenceNeoplasm InvasivenessNeoplasms, ExperimentalNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAntigens, Tumor-Associated, CarbohydrateCMP-N-acetylneuraminate-alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferaseNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktsialosyl-Tn antigenSialyltransferasesHepatocarcinomaInvasionMigrationProliferationST6GalNAc ISTn

Identifiers

PMID27235117
OpenAlexW2404940319

What OpenQuestion holds

Textmetadata
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.