Evidence map›Paper›PMID 26261530›Full record

ArticleInternational journal of clinical and experimental pathology2015

Protective effect of RIP and c-FLIP in preventing liver cancer cell apoptosis induced by TRAIL.

Jichun Sun, Hongwu Luo, Wanpin Nie, Xundi Xu, Xiongying Miao, Feizhou Huang, Haiyan Wu, Xiaoxin Jin

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. RIP-1/c-FLIPL Induce Hepatic Cancer Cell Apoptosis Through Regulating Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand (TRAIL).Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  5. Article
  6. Article
  7. Article
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 1 institution in 1 country.

Jichun SunDepartment of Surgery, The 3rd Xiangya Hospital, Central South University Changsha, Hunan Province, China.
Hongwu LuoDepartment of Surgery, The 3rd Xiangya Hospital, Central South University Changsha, Hunan Province, China.
Wanpin NieDepartment of Surgery, The 3rd Xiangya Hospital, Central South University Changsha, Hunan Province, China.
Xundi XuDepartment of Surgery, The Second Xiangya Hospital, Central South University Changsha, Hunan Province, China.
Xiongying MiaoDepartment of Surgery, The Second Xiangya Hospital, Central South University Changsha, Hunan Province, China.
Feizhou HuangDepartment of Surgery, The 3rd Xiangya Hospital, Central South University Changsha, Hunan Province, China.
Haiyan WuDepartment of Surgery, The 3rd Xiangya Hospital, Central South University Changsha, Hunan Province, China.
Xiaoxin JinDepartment of Surgery, The Second Xiangya Hospital, Central South University Changsha, Hunan Province, China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TRAIL (TNF-related apoptosis-inducing ligand) is a member of the tumor necrosis factor superfamily that can induce tumor selective death by up-regulating death receptor 4 (DR4) and DR5 expression. The study aimed to explore the role of RIP and c-FLIP genes in TRAIL induced liver cancer cell HepG2 and Hep3B apoptosis and related mechanism. RIP and c-FLIP silenced HepG2 and Hep3B cell model were established through siRNA. Western blot was applied to test c-FLIP, RIP, DR4, DR5, FADD, Caspase-3/8/9, ERK1/2, and DFF45 protein expression. Caspase-8 kit was used to detect Caspase-8 expression. Flow cytometry was performed to measure cell apoptosis rate. Acid phosphatase method was applied to determine cell cycle. TRAIL had no significant effect on Caspase-3/8/9, DR4, DR5, ERK1/2, and DFF45 protein expression, but up-regulated c-FLIP and RIP protein expression and reduced FADD expression level. After treated by the chemotherapy drug mitomycin and adriamycin, c-FLIP and RIP expression decreased significantly, while FADD increased. After knockout c-FLIP and RIP gene, HepG2 and Hep3B cell apoptosis rate induced by TRAIL increased obviously. Meanwhile, cell subG1 percentage increased markedly and exhibited G1 phase growth retardation. In addition, after two kinds of gene knockout, Caspase-8 was activated and produce Caspase-3 P20 and P24, leading DFF45 appeared DNA fragment P17 and P25. c-FLIP and RIP can inhibit Caspase-8 activation and prompting HepG2 and Hep3B resistant to cell apoptosis induced by TRAIL.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsApoptosisCASP8 and FADD-Like Apoptosis Regulating ProteinCaspase 8Dose-Response Relationship, DrugDrug Resistance, NeoplasmEnzyme ActivationG1 Phase Cell Cycle CheckpointsHep G2 CellsHumansLiver NeoplasmsReceptor-Interacting Protein Serine-Threonine KinasesRNA InterferenceSignal TransductionTime FactorsTNF-Related Apoptosis-Inducing LigandCASP8 and FADD-Like Apoptosis Regulating ProteinCASP8 protein, humanCaspase 8CFLAR protein, humanReceptor-Interacting Protein Serine-Threonine KinasesTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanapoptosisc-FLIPliver cancerRIPTRAIL

Identifiers

PMID26261530
PMCPMC4525864
OpenAlexW2402406506

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.