Evidence map›Paper›PMID 29347944›Full record

ArticleWorld journal of surgical oncology2018

Expression of UGP2 and CFL1 expression levels in benign and malignant pancreatic lesions and their clinicopathological significance.

Lingxiang Wang, Li Xiong, Zhengchun Wu, Xiongying Miao, Ziru Liu, Daiqiang Li, Qiong Zou, Zhulin Yang

Open access · goldAbstract read
In one paragraph

Article in World journal of surgical oncology, 2018. 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
1.5field-weighted citation impact, top 14% 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, 30 citations in OpenAlex.

  1. Review
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  12. UDP-glucose pyrophosphorylase 2, a regulator of glycogen synthesis and glycosylation, is critical for pancreatic cancer growth.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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

8 authors at 2 institutions in 1 country.

Lingxiang WangGeneral Surgery Department, Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, People's Republic of China.
Li XiongGeneral Surgery Department, Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, People's Republic of China.
Zhengchun WuGeneral Surgery Department, Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, People's Republic of China.
Xiongying MiaoGeneral Surgery Department, Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, People's Republic of China.
Ziru LiuGeneral Surgery Department, Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, People's Republic of China.
Daiqiang LiDepartment of Pathology, Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, People's Republic of China.
Qiong ZouDepartment of Pathology, Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, People's Republic of China.
Zhulin YangGeneral Surgery Department, Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, People's Republic of China. 4896142@qq.com.
Central South University · CNSecond Xiangya Hospital of Central South University · CN

Funding

Changsha Science and Technology Plan K1205018-31Innovation Project of Ministry of Science and Technology No. X8C1Y0K9National Natural Science Foundation of China Nos. 81472738, 81372628, 81402536, 31571241, 31660266Planned Science and Technology Project of Hunan province No. 2015GK3117, 2014WK2016
6 · The paper itself

Abstract

backgroundThis study investigated UGP2 (uridine diphosphate-glucose pyrophosphorylase-2) and CFL1 (cofilin-1) expression in pancreatic ductal carcinoma (PDC), paracancerous tissue (PT), benign lesions (BL), and normal tissue (NT) and their clinicopathological significance.

methodsSurgical specimens, which were collected from 106 cases of pancreatic ductal carcinoma, 35 cases of paracancerous tissues, 55 cases of benign lesions and 13 cases of normal pancreatic tissues, were fixed with 4% formaldehyde to prepare conventional paraffin-embedded sections. EnVision immunohistochemical was used to stain for UGP2 and CFL1. Kaplan-Meier survival analysis was performed to assess the correlation of expression pattern with survival.

resultsWe found that positive UGP2 and CFL1 expression in PDC were significantly higher than those in PT, BL, and NT. In PT and BL with positive UGP2 and CFL1 expression, mild to severe atypical hyperplasia or intraepithelial neoplasia of grades II-III was observed in ductal epithelium. Positive UGP2 and CFL1 expression in cases with high differentiation, no lymph node metastasis, no surrounding invasion, and TNM (tumor-node-metastasis) staging I or/and II were significantly lower than those in cases with poor differentiation, lymph node metastasis, surrounding invasion, and TNM stage III and/or IV. Positive UGP2 expression in male patients was significantly lower than that in female patients. UGP2 and CFL1 expression in PDC were positively correlated. Kaplan-Meier survival analysis showed the degree of differentiation, tumor maximal diameter, TNM stage, lymph node metastasis, and surrounding invasion, and UGP2 and CFL1 expression were closely related to the average survival time of patients with PDC. The survival time of patients with positive UGP2 and CFL1 expression was significantly shorter than that of patients with negative expression. Cox multivariate analysis showed that poor differentiation, tumor maximal diameter ≥ 3 cm, TNM stage III or IV, lymph node metastasis, surrounding invasion, and positive UGP2 and CFL1 expression was negatively correlated with the postoperative survival rate and positively correlated with the mortality of patients with PDC.

conclusionPositive expression of UGP2 and CFL1 can serve a valuable prognostic factor in pancreatic cancer.

Indexed as

AdenocarcinomaBiomarkers, TumorCarcinoma, Pancreatic DuctalCase-Control StudiesCofilin 1FemaleFollow-Up StudiesHumansLymphatic MetastasisMaleMiddle AgedNeoplasm InvasivenessPancreasPancreatic NeoplasmsPrognosisSurvival RateBiomarkers, TumorCFL1 protein, humanCofilin 1UTP-Glucose-1-Phosphate UridylyltransferaseCFL1Chronic pancreatitisPancreatic ductal adenocarcinomaPancreatic intraepithelial neoplasiaUGP2

Identifiers

PMID29347944
PMCPMC5774110
OpenAlexW2796412139

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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.