Evidence map›Paper›PMID 27604096›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2017

Synergistic antitumor efficacy of antibacterial helvolic acid from Cordyceps taii and cyclophosphamide in a tumor mouse model.

Jian-Hui Xiao, Yao Zhang, Gui-You Liang, Ru-Ming Liu, Xiao-Gang Li, Ling-Tao Zhang, Dai-Xiong Chen, Jian-Jiang Zhong

Open access · greenAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.1field-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

10 citing papers in PubMed, 18 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.

Jian-Hui Xiao1 Centre for Translational Medicinal of Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, PR China.
Yao Zhang1 Centre for Translational Medicinal of Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, PR China.
Gui-You Liang1 Centre for Translational Medicinal of Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, PR China.
Ru-Ming Liu1 Centre for Translational Medicinal of Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, PR China.
Xiao-Gang Li1 Centre for Translational Medicinal of Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, PR China.
Ling-Tao Zhang1 Centre for Translational Medicinal of Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, PR China.
Dai-Xiong Chen1 Centre for Translational Medicinal of Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, PR China.
Jian-Jiang Zhong2 State Key Laboratory of Microbial Metabolism, and School of Life Science & Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, PR China.
Zunyi Medical University · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The antibacterial agent helvolic acid, which was isolated from the active antitumor fraction of Cordyceps taii, showed potent cytotoxicity against different human cancer cells. In the present study, the in vivo antitumor effect of helvolic acid was investigated in murine sarcoma S180 tumor-bearing mice. Doses of 10 and 20 mg/kg/day helvolic acid did not exert significant antitumor activity. Interestingly, co-administration of 10 mg/kg/day helvolic acid and 20 mg/kg/day cyclophosphamide (CTX) - a well-known chemotherapy drug - showed promising antitumor activity with a growth inhibitory rate of 70.90%, which was much higher than that of CTX alone (19.5%). Furthermore, the combination markedly prolonged the survival of tumor-bearing mice. In addition, helvolic acid enhanced the immune organ index. The protein expression levels of β-catenin, cyclin D1, and proliferating cell nuclear antigen were significantly suppressed in mice treated with 20 mg/kg/day helvolic acid and in those receiving combination therapy. Taken together, these results indicated that helvolic acid in combination with CTX showed potent in vivo synergistic antitumor efficacy, and its mechanism of action may involve the Wnt/ β-catenin signaling pathway.

Indexed as

AnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy Protocolsbeta CateninCell Line, TumorCordycepsCyclin D1CyclophosphamideDisease Models, AnimalDrug SynergismFusidic AcidMaleMiceProliferating Cell Nuclear AntigenSarcomaWnt ProteinsAntineoplastic Agentsbeta CateninCcnd1 protein, mouseCyclin D1CyclophosphamideFusidic Acidhelvolic acidProliferating Cell Nuclear AntigenWnt Proteinsantitumor activityCordyceps taiicyclophosphamidehelvolic acidmechanism of actionMedicinal mushroomsynergistic effect

Identifiers

PMID27604096
PMCPMC5167114
OpenAlexW2514944617

What OpenQuestion holds

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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.