Evidence map›Paper›PMID 25321475›Full record

ArticleCell death & disease2014

Contribution of TIP30 to chemoresistance in laryngeal carcinoma.

M Zhu, F Yin, L Yang, S Chen, R Chen, X Zhou, W Jing, X Fan, R Jia, H Wang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  14. Gigantol Suppresses Cancer Stem Cell-Like Phenotypes in Lung Cancer Cells.Evidence-based complementary and alternative medicine : eCAM · 2015
    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

13 authors at 3 institutions in 1 country.

M Zhu1] International Joint Cancer Research Institute, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China [2] Changhai Hospital, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
F Yin1] International Joint Cancer Research Institute, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China [2] PLA General Hospital Cancer Center, PLA Postgraduate School of Medicine, 28 Fuxing Road, Beijing, People's Republic of China.
L YangChanghai Hospital, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
S ChenChanghai Hospital, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
R ChenInternational Joint Cancer Research Institute, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
X ZhouChanghai Hospital, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
W JingChanghai Hospital, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
X FanInternational Joint Cancer Research Institute, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
R JiaInternational Joint Cancer Research Institute, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
H WangInternational Joint Cancer Research Institute, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
H ZhengChanghai Hospital, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China.
J Zhao1] International Joint Cancer Research Institute, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China [2] PLA General Hospital Cancer Center, PLA Postgraduate School of Medicine, 28 Fuxing Road, Beijing, People's Republic of China.
Y Guo1] International Joint Cancer Research Institute, The Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People's Republic of China [2] PLA General Hospital Cancer Center, PLA Postgraduate School of Medicine, 28 Fuxing Road, Beijing, People's Republic of China.
Second Military Medical University · CNChanghai Hospital · CNChinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Laryngeal squamous cell carcinoma (LSCC) is one of the most common carcinomas of the head and neck. Despite advances in diagnosis and treatment, the survival of patients with LSCC has not improved in the past two decades. TIP30, a newly identified tumour suppressor, appears to be involved in multiple processes during tumour development. Here, we investigated the involvement of TIP30 in chemoresistance of LSCC in vitro and in vivo. We showed that TIP30 expression decreased significantly in drug-selected cells (DSCs) of laryngeal carcinoma. Suppressing TIP30 enhanced resistance capability to multiple chemotherapy drugs, cell proliferation and self-renewal in Hep2 cells. Additionally, decreased self-renewal capacity and chemotherapeutic resistance were observed in DSCs overexpressing TIP30. Furthermore, TIP30 negatively regulated tumourigenesis and chemoresistance in LSCC cells subcutaneously transplanted into nude mice. Moreover, decreased TIP30 expression contributed to chemoresistance, self-renewal and proliferation of LSCC cells via nuclearlisation of β-catenin, a cell-cell adhesion and stem cell renewal regulator. Consistently, Kaplan-Meier and Cox proportional hazards regression modelling analyses showed that decreased TIP30 expression independently predicted poor survival in patients with LSCC. Taken together, our results reveal that TIP30 has a crucial role in chemoresistance of LSCC through the AKT/glycogen synthase kinase-3β/β-catenin signalling pathway and may be a promising candidate for improving LSCC chemotherapy.

Indexed as

Drug Resistance, NeoplasmAcetyltransferasesAgedAnimalsbeta CateninCarcinogenesisCell AdhesionCell Line, TumorCell ProliferationFemaleGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHumansImmunohistochemistryLaryngeal NeoplasmsMaleAcetyltransferasesbeta CateninGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGSK3B protein, humanGsk3b protein, mouseHTATIP2 protein, humanProto-Oncogene Proteins c-aktTranscription Factors

Identifiers

PMID25321475
PMCPMC4237250
OpenAlexW1978965943

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.