Evidence map›Paper›PMID 36454514›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2023

Nucleotide sugar transporter SLC35A2 is involved in promoting hepatocellular carcinoma metastasis by regulating cellular glycosylation.

Hongxia Cheng, Sikai Wang, Dongmei Gao, Kangkang Yu, Huaping Chen, Yilan Huang, Miaomiao Li, Jubo Zhang, Kun Guo

Abstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed, 19 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Hongxia ChengLiver Cancer Institute, Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Zhongshan Hospital, Building19, No. 180, Fenglin Road, 20032, Shanghai, People's Republic of China.
Sikai WangLiver Cancer Institute, Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Zhongshan Hospital, Building19, No. 180, Fenglin Road, 20032, Shanghai, People's Republic of China.
Dongmei GaoLiver Cancer Institute, Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Zhongshan Hospital, Building19, No. 180, Fenglin Road, 20032, Shanghai, People's Republic of China.
Kangkang YuDepartment of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, People's Republic of China.
Huaping ChenDepartment of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Yilan HuangLiver Cancer Institute, Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Zhongshan Hospital, Building19, No. 180, Fenglin Road, 20032, Shanghai, People's Republic of China.
Miaomiao LiLiver Cancer Institute, Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Zhongshan Hospital, Building19, No. 180, Fenglin Road, 20032, Shanghai, People's Republic of China.
Jubo ZhangDepartment of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, People's Republic of China. drzhangjubo@163.com.
Kun GuoLiver Cancer Institute, Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Zhongshan Hospital, Building19, No. 180, Fenglin Road, 20032, Shanghai, People's Republic of China. guo.kun@zs-hospital.sh.cn.
Zhongshan Hospital · CNFudan University · CNGuangxi Medical University · CN

Funding

National Natural Science Foundation of China 81872492
6 · The paper itself

Abstract

purposeRecently, aberrant glycosylation has been recognized to be relate to malignant behaviors of cancer and outcomes of patients with various cancers. SLC35A2 plays an indispensable role on glycosylation as a nucleotide sugar transporter. However, effects of SLC35A2 on malignant behaviors of cancer cells and alteration of cancer cells surface glycosylation profiles are still not fully understood, particularly in hepatocellular carcinoma (HCC). Hence, from a glycosylation perspective, we investigated the effects of SLC35A2 on metastatic behaviors of HCC cells.

methodsSLC35A2 expression in clinical samples and HCC cells was examined by immunohistochemical staining or Western blot/quantitative PCR and was regulated by RNA interference or vectors-mediated transfection. Effects of SLC35A2 expression alteration on metastatic behaviors and membrane glycan profile of HCC cells were observed by using respectively invasion, migration, cell adhesion assay, in vivo lung metastatic nude mouse model and lectins microarray. Co-location among proteins in HCC cells was observed by fluorescence microscope and detected by an in vitro co-immunoprecipitation assay.

resultsSLC35A2 was upregulated in HCC tissues, and is associated with poor prognosis of HCC patients. SLC35A2 expression alteration significantly affected the invasion, adhesion, metastasis and membrane glycan profile and led to the dysregulated expressions or glycosylation of cell adhesion-related molecules in HCC cells. Mechanistically, the maintenance of SLC35A2 activity is critical for the recruitment of the key galactosyltransferase B4GalT1, which is responsible for complex glycoconjugate and lactose biosynthesis, to Golgi apparatus in HCC cells.

conclusionSLC35A2 plays important roles in promoting HCC metastasis by regulating cellular glycosylation modification and inducing the cell adhesive ability of HCC cells.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMonosaccharide Transport ProteinsNucleotide Transport ProteinsAnimalsCell Line, TumorCell MovementGene Expression Regulation, NeoplasticGlycosylationHumansMiceNeoplasm InvasivenessNeoplasm MetastasisNucleotidesPolysaccharidesSugarsMonosaccharide Transport ProteinsNucleotidesNucleotide Transport ProteinsPolysaccharidesSugarsUDP-Galactose TranslocatorsB4GalT1GlycosylationHepatocellular carcinomaMetastasisSLC35A2

Identifiers

PMID36454514
PMCPMC12974757
OpenAlexW4310565735

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.