Evidence map›Paper›PMID 28797103›Full record

ArticlePloS one2017

Effects of cancer-testis antigen, TFDP3, on cell cycle regulation and its mechanism in L-02 and HepG2 cell lines in vitro.

Yunshen Jiao, Lingyu Ding, Ming Chu, Tieshan Wang, Jiarui Kang, Xiaofan Zhao, Huanhuan Li, Xi Chen, Zirui Gao, Likai Gao and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

6 citing papers in PubMed, 9 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

11 authors at 3 institutions in 1 country.

Yunshen JiaoDepartment of Immunology, School of Basic Medical Science, Peking University, Beijing, China.
Lingyu DingDepartment of Immunology, School of Basic Medical Science, Peking University, Beijing, China.
Ming ChuDepartment of Immunology, School of Basic Medical Science, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-0507-9569
Tieshan WangBeijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Jiarui KangDepartment of Pathology, the First Affiliated Hospital of General Hospital of Chinese People's Liberation Army, Beijing, China.
Xiaofan ZhaoDepartment of Immunology, School of Basic Medical Science, Peking University, Beijing, China.
Huanhuan LiDepartment of Immunology, School of Basic Medical Science, Peking University, Beijing, China.
Xi ChenDepartment of Immunology, School of Basic Medical Science, Peking University, Beijing, China.
Zirui GaoDepartment of Immunology, School of Basic Medical Science, Peking University, Beijing, China.
Likai GaoDepartment of Immunology, School of Basic Medical Science, Peking University, Beijing, China.
Yuedan WangDepartment of Immunology, School of Basic Medical Science, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-9662-1025
Peking University · CNBeijing University of Chinese Medicine · CNFirst Affiliated Hospital of Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TFDP3, also be known as HCA661, was one of the cancer-testis antigens, which only expressed in human tissues. The recent researches about TFDP3 mostly focused on its ability to control the drug resistance and apoptosis of tumor cells. However, the role of TFDP3 in the progress of the cell cycle is rarely involved. In this study, we examined the expression of TFDP3 in human liver tissues firstly. After that, we detect the expression of TFDP3 at the RNA level and protein level in L-02 cell line and HepG2 cell line, and the location of TFDP3 was defined by immunofluorescence technique. Furthermore, we synchronized the cells to G1 phase, S phase and G2 phase, and arrested cell mitosis. The localization of TFDP3 and co-localization with E2F1 molecules in different phases of hepatocyte lines. Finally, TFDP3 gene knockout was performed on L-02 and HepG2 cell lines, and detected the new cell cycles by flow cytometry. The result showed that the expression of TFDP3 molecule is negative in normal liver tissue, but positive in immortalized human hepatocyte cell line, and the expression level is lower than in hepatocellular carcinoma cell line. The expression level of TFDP3 was in the dynamic change of L-02 and HepG2 cell lines, and was related to the phase transition. TFDP3 can bind to E2F1 molecule to form E2F/TFDP3 complex; and the localizations of TFDP3 and E2F1 molecules and the co-localization were different in different phases of cell cycle in the nucleus and cytoplasm, which indicated that the E2F/TFDP3 complex involved in the process of regulating the cell cycle. By knocking down the TFDP3 expression level in L-02 and HepG2 cell lines, the cell cycle would be arrested in S phase, which confirmed that TFDP3 can be a potential target for tumor therapy.

Indexed as

S Phase Cell Cycle CheckpointsCarcinoma, HepatocellularE2F1 Transcription FactorHep G2 CellsHumansLiverLiver NeoplasmsMaleTestisTranscription Factor DP1E2F1 protein, humanE2F1 Transcription FactorTFDP3 protein, humanTranscription Factor DP1

Identifiers

PMID28797103
PMCPMC5552311
OpenAlexW2743708607

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Registered trials

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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.