Evidence map›Paper›PMID 26121319›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2015

Overexpression of SULT2B1b is an independent prognostic indicator and promotes cell growth and invasion in colorectal carcinoma.

Liang Hu, Guang-Zhen Yang, Yu Zhang, Dan Feng, Yan-Xia Zhai, Hui Gong, Chen-Ye Qi, Hao Fu, Ming-Ming Ye, Qing-Ping Cai and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

20 citing papers in PubMed, 28 citations in OpenAlex.

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  6. Human sulfotransferaseFrontiers in genetics · 2024
    Review
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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

11 authors at 3 institutions in 1 country.

Liang HuAnal-Colorectal Surgery Institute, 150th Hospital of PLA, Luoyang, China.
Guang-Zhen YangAnal-Colorectal Surgery Institute, 150th Hospital of PLA, Luoyang, China.
Yu ZhangAnal-Colorectal Surgery Institute, 150th Hospital of PLA, Luoyang, China.
Dan FengDepartment of Oncology, Changhai Hospital, Second Military Medical University, Shanghai, China.
Yan-Xia ZhaiAnal-Colorectal Surgery Institute, 150th Hospital of PLA, Luoyang, China.
Hui GongAnal-Colorectal Surgery Institute, 150th Hospital of PLA, Luoyang, China.
Chen-Ye QiAnal-Colorectal Surgery Institute, 150th Hospital of PLA, Luoyang, China.
Hao FuAnal-Colorectal Surgery Institute, 150th Hospital of PLA, Luoyang, China.
Ming-Ming YeAnal-Colorectal Surgery Institute, 150th Hospital of PLA, Luoyang, China.
Qing-Ping CaiDepartment of Gastrointestine Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Chun-Fang GaoAnal-Colorectal Surgery Institute, 150th Hospital of PLA, Luoyang, China.
82th Hospital of Pla · CNChanghai Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant expression of cytosolic sulfotransferase 2B1b (SULT2B1b) has been reported in several human malignancies. However, the expression pattern and clinical significance of SULT2B1b in colorectal carcinoma (CRC) remains unknown. Real-time quantitative PCR, western blot, and immunohistochemistry analyses were used to determine SULT2B1b expression in CRC clinical samples and CRC-derived cell lines. Kaplan-Meier and Cox proportional regression analyses were used to evaluate the association between SULT2B1b expression and patient survival in two independent cohorts of 485 patients with CRC. Gain- and loss-of-function approaches were employed to investigate the role of SULT2B1b in regulation of CRC cell growth and invasion. We found that SULT2B1b expression was frequently upregulated in CRC clinical samples and CRC-derived cell lines and was significantly correlated with lymph node metastasis and TNM stage in both the training and validation cohorts. Patients with higher intratumoral SULT2B1b expression had a significantly shorter disease-specific survival (DSS) and disease-free survival (DFS) than those with lower expression. Importantly, increased expression of SULT2B1b significantly predicted poor DSS and DFS and was an independent unfavorable prognostic indicator for stage II patients in both cohorts. Functional studies revealed that overexpression of SULT2B1b promoted CRC cell growth and invasion in vitro. Conversely, knockdown of SULT2B1b inhibited these processes. In conclusion, our findings suggest that SULT2B1b expression correlates with disease progression and metastasis and may serve as a novel prognostic biomarker and potential therapeutic target for patients with CRC.

Indexed as

Blotting, WesternCell ProliferationColorectal NeoplasmsGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansImmunohistochemistryKaplan-Meier EstimateNeoplasm InvasivenessPrognosisReal-Time Polymerase Chain ReactionRegression AnalysisSulfotransferasesSulfotransferasesSULT2B1 protein, human

Identifiers

PMID26121319
PMCPMC4558402
OpenAlexW1579864275

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.