Evidence map›Paper›PMID 35234600›Full record

ArticleParasitology2022

Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta as a potential biomarker for

Sattrachai Prasopdee, Yodying Yingchutrakul, Sittiruk Roytrakul, Montinee Pholhelm, Teva Phanaksri, Anthicha Kunjantarachot, Jutharat Kulsantiwong, Kritiya Butthongkomvong, Smarn Tesana, Thanakrit Sathavornmanee and 1 more

Open access · greenAbstract read
In one paragraph

Article in Parasitology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. 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

11 authors at 5 institutions in 1 country.

Sattrachai PrasopdeeThammasat University Research Unit in Opisthorchiasis, Cholangiocarcinoma, and Neglected Parasitic Diseases, Thammasat University, Pathum Thani, 12120, Thailand.
Yodying YingchutrakulProteomics Research Team, National Omics Center, NSTDA, Pathum Thani, 12120, Thailand.
Sittiruk RoytrakulProteomics Research Laboratory, National Center for Genetic Engineering and Biotechnology (BIOTEC), NSTDA, Pathum Thani, 12120, Thailand.
Montinee PholhelmChulabhorn International College of Medicine, Thammasat University, Pathum Thani, 12120, Thailand.
Teva PhanaksriChulabhorn International College of Medicine, Thammasat University, Pathum Thani, 12120, Thailand.
Anthicha KunjantarachotChulabhorn International College of Medicine, Thammasat University, Pathum Thani, 12120, Thailand.
Jutharat KulsantiwongFaculty of Science, Udon Thani Rajabhat University, Udon Thani, 41000, Thailand.
Kritiya ButthongkomvongMedical Oncology Unit, Udonthani Cancer Hospital, Udon Thani, 41330, Thailand.
Smarn TesanaChulabhorn International College of Medicine, Thammasat University, Pathum Thani, 12120, Thailand.
Thanakrit SathavornmaneeChonburi hospital, Ministry of Public Health, Chonburi, 20000, Thailand.
Veerachai ThitapakornThammasat University Research Unit in Opisthorchiasis, Cholangiocarcinoma, and Neglected Parasitic Diseases, Thammasat University, Pathum Thani, 12120, Thailand.ORCID 0000-0001-9350-2146
Thammasat University · THNational Science and Technology Development Agency · THMinistry of Public Health · THUdon Thani Hospital · THUdon Thani Rajabhat University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human liver fluke Opisthorchis viverrini (Ov), the primary risk factor for cholangiocarcinoma (CHCA), is a parasite endemic to southeast Asian countries. With no effective treatments for CHCA currently available, early diagnosis and treatment of Ov infection remains the only practical method for the prevention of CHCA. In this study, plasma phosphoproteomes of patients in the non-Ov infection, non-cholangiocarcinoma subject group (non-OVCCA), the asymptomatic Ov infected group (OV), and the CHCA group (CCA), were investigated to identify potential biomarkers for Ov infection and CHCA. The AKT signalling pathway was found to be up-regulated. Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform (PIK3CB), an upstream signalling molecule, was selected as a potential biomarker and evaluated using indirect enzyme-linked immunosorbent assay (ELISA). Results demonstrated evidence that levels of PIK3CB in both the OV group and CCA group was statistically different compared to the non-OVCCA group (P < 0.01). However, the levels of PIK3CB between the OV group and the CCA group were found not to be statistically different. Sensitivity and specificity for OV using OD450 cut-off at >1.570 was 76 and 72%, respectively. For CCA, sensitivity and specificity using OD450 cut-off at >1.398 was 68 and 76%, respectively. Application of indirect ELISA detecting plasma PIK3CB will be of great benefit for screening of opisthorchiasis and CHCA.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaOpisthorchiasisOpisthorchisAnimalsBile Ducts, IntrahepaticBiomarkersCatalytic DomainHumansPhosphatidylinositolsBiomarkersPhosphatidylinositolsBiomarkercholangiocarcinomadiagnosisOpisthorchis viverriniPhosphoproteomePIK3CB

Identifiers

PMID35234600
PMCPMC11010463
OpenAlexW3203668128

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.