Evidence map›Paper›PMID 27021903›Full record

ArticleBMC cancer2016

Antitumor effects of cecropin B-LHRH' on drug-resistant ovarian and endometrial cancer cells.

Xiaoyong Li, Bo Shen, Qi Chen, Xiaohui Zhang, Yiqing Ye, Fengmei Wang, Xinmei Zhang

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 27 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

7 authors at 2 institutions in 1 country.

Xiaoyong LiDepartment of Gynecology, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Bo ShenInstitute of Radiation Medicine, Fudan University, Shanghai, China.
Qi ChenCentral Laboratory, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Xiaohui ZhangDepartment of Women Health Care, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yiqing YePharmacy Division, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Fengmei WangPharmacy Division, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Xinmei ZhangDepartment of Gynecology, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China. xinmeizhangsci@126.com.
Women's Hospital, School of Medicine, Zhejiang University · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLuteinizing hormone-releasing hormone receptor (LHRHr) represents a promising therapeutic target for treating sex hormone-dependent tumors. We coupled cecropin B, an antimicrobial peptide, to LHRH', a form of LHRH modified at carboxyl-terminal residues 4-10, which binds to LHRHr without interfering with luteinizing hormone (LH) and follicle-stimulating hormone (FSH) secretion. This study aimed to assess the antitumor effects of cecropin B-LHRH' (CB-LHRH') in drug-resistant ovarian and endometrial cancers.

methodsTo evaluate the antitumor effects of CB-LHRH', three drug resistant ovarian cancer cell lines (SKOV-3, ES-2, NIH:OVCAR-3) and an endometrial cancer cell line (HEC-1A) were treated with CB-LHRH'. Cell morphology changes were assessed using inverted and electron microscopes. In addition, cell growth and cell cytotoxicity were measured by MTT assay and LDH release, respectively. In addition, hemolysis was measured. Furthermore, radioligand receptor binding, hypersensitization and minimal inhibitory concentrations (against Staphylococcus aureus, Klebsiella pneumoniae, Escherichia coli, Enterobacter cloacae, Pseudomonas aeruginosa, and Acinetobacter baumannii) were determined. Finally, the impact on tumor growth in BALB/c-nu mice was assessed in an ES-2 xenograft model.

resultsCB-LHRH' bound LHRHr with high-affinity (dissociation constant, Kd = 0.252 ± 0.061 nM). Interestingly, CB-LHRH' significantly inhibited the cell viability of SKOV-3, ES-2, NIH:OVCAR-3 and HEC-1A, but not that of normal eukaryotic cells. CB-LHRH' was active against bacteria at micromolar concentrations, and caused no hypersensitivity in guinea pigs. Furthermore, CB-LHRH' inhibited tumor growth with a 23.8 and 20.4 % reduction in tumor weight at 50 and 25 mg/kg.d, respectively.

conclusionsCB-LHRH' is a candidate for targeted chemotherapy against ovarian and endometrial cancers.

Indexed as

AnimalsAntineoplastic AgentsAntineoplastic Agents, HormonalCecropinsCell Line, TumorCell ProliferationDoxorubicinDrug Resistance, NeoplasmEndometrial NeoplasmsFemaleGonadotropin-Releasing HormoneHumansMiceOvarian NeoplasmsXenograft Model Antitumor AssaysAntineoplastic AgentsAntineoplastic Agents, HormonalCecropinsDoxorubicinGonadotropin-Releasing HormoneCecropin B peptideEndometrial cancerLuteinizing hormone releasing-hormone receptorOvarian cancer

Identifiers

PMID27021903
PMCPMC4809036
OpenAlexW2305789994

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.