Evidence map›Paper›PMID 24040444›Full record

ArticleInternational journal of clinical and experimental pathology2013

Growth inhibitory effect of Cucurbitacin E on breast cancer cells.

Tian Lan, Linling Wang, Qian Xu, Weiguo Liu, Hongchuan Jin, Weimin Mao, Xian Wang, Xiaojia Wang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 40 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

8 authors at 2 institutions in 1 country.

Tian LanDepartment of Medical Oncology, the key laboratory of Integrated Chinese and Western Medical Oncology in Zhejiang Province, Zhejiang Cancer Hospital HangZhou, China 310022 ; Department of Medical Oncology, Institute of Clinical Science, Sir Runrun Shaw Hospital, Medical College of Zhejiang University Hangzhou, China 310003.
Linling Wang
Qian Xu
Weiguo Liu
Hongchuan Jin
Weimin Mao
Xian Wang
Xiaojia Wang
Sir Run Run Shaw Hospital · CNZhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDue its inhibitory effects on chemical carcinogenesis and inflammation, Cucurbitacins have been proposed as an effective agent for the prevention or treatment of human cancers. In this study, we aimed to explore the effect of Cucurbitacin E (CuE) on human breast cancer cells.

methodsThe inhibitory effect of CuE on proliferation of Bcap37 and MDA-MB-231 cells was assessed by MTT assay. The cell cycle distribution and cell apoptosis were determined by flow cytometry (FCM). The expression of pro-caspase 3, cleaved caspase 3, p21, p27 and the phosphorylation of signaling proteins was detected by Western Blotting.

resultsCuE inhibited the growth of human breast cancer cells in a dose and time-dependent manner. FCM analysis showed that CuE induced G2/M phase arrest and cell apoptosis. CuE treatment promoted the cleavage of caspase 3 and upregulated p21 and p27. In addition, the phosphorylation of STAT3 but not ERK-1/2 was abrogated upon CuE treatment. Interestingly, losedose CuE significantly enhanced the growth inhibition induced by cisplatin. Conclusions Cucurbitacin E (CuE) could inhibit the growth of human breast cancer cells in vitro. CuE induced both apoptosis and cell cycle arrest probably through the inhibition of STAT3 function. Lose-dose CuE significantly enhanced the growth inhibitory effect of cisplatin on breast cancer cells, further indicating the potential clinical values of CuE for the prevention or treatment of human breast cancer.

Indexed as

Antineoplastic Agents, PhytogenicAntineoplastic Combined Chemotherapy ProtocolsApoptosisBreast NeoplasmsCaspase 3Cell Cycle CheckpointsCell Line, TumorCell ProliferationCisplatinCyclin-Dependent Kinase Inhibitor p21Cyclin-Dependent Kinase Inhibitor p27Dose-Response Relationship, DrugDrug SynergismExtracellular Signal-Regulated MAP KinasesFemaleHumansAntineoplastic Agents, PhytogenicCASP3 protein, humanCaspase 3CDKN1A protein, humanCDKN1B protein, humanCisplatincucurbitacin ECyclin-Dependent Kinase Inhibitor p21Cyclin-Dependent Kinase Inhibitor p27Extracellular Signal-Regulated MAP KinasesPHB2 protein, humanProhibitinsSTAT3 protein, humanSTAT3 Transcription FactorTriterpenesapoptosisbreast cancerCucurbitacin E

Identifiers

PMID24040444
PMCPMC3759486
OpenAlexW1572672818

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.