Evidence map›Paper›PMID 25550798›Full record

ArticleInternational journal of clinical and experimental pathology2014

Effect of celecoxib combined with chemotherapy drug on malignant biological behaviors of gastric cancer.

Cuicui Meng, Zhonghua Lu, Mingming Fang, Xifa Zhou, Kejun Dai, Shuyu Zhang, Judong Luo, Zhibin Luo

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

0 citing papers in PubMed, 8 citations in OpenAlex.

No citing paper in PubMed yet.

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.

Cuicui MengDepartment of Radiotherapy, Changzhou Cancer Hospital, Soochow University Changzhou 213001, China.
Zhonghua LuDepartment of Radiotherapy, Changzhou Cancer Hospital, Soochow University Changzhou 213001, China.
Mingming FangDepartment of Radiotherapy, Changzhou Cancer Hospital, Soochow University Changzhou 213001, China.
Xifa ZhouDepartment of Radiotherapy, Changzhou Cancer Hospital, Soochow University Changzhou 213001, China.
Kejun DaiDepartment of Radiotherapy, Changzhou Cancer Hospital, Soochow University Changzhou 213001, China.
Shuyu ZhangSchool of Radiation Medicine and Protection and Jiangsu Provincial Key Laboratory of Radiation Medicine and Protection, Soochow University Suzhou 215123, China.
Judong LuoDepartment of Radiotherapy, Changzhou Cancer Hospital, Soochow University Changzhou 213001, China.
Zhibin LuoDepartment of Oncology, Third People's Hospital of Chongqing Chongqing 400016, China.
Soochow University · CNThird People 's Hospital of Chongqing · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Celecoxib, a selective cyclooxygenase-2 (COX-2) inhibitor, has been reported to have antitumor effects. In some tumor models, the combination of celecoxib with chemotherapy agents has shown synergistic antitumor effect; however, the effect of celecoxib combination with tegafur/gimeracil/oteracil potassium on the malignant biological behaviors of gastric cancer in nude mice is unclear. In this study, female nude mice were subcutaneously transplanted with SGC-7901 gastric cancer cells. When the tumor model formed, the mice were divided into control group, celecoxib group, tegafur/gimeracil/oteracil potassium group, and the combination of both drug regimens group. Mice were treated for 3 weeks. Following treatment, the proliferating index was calculated, apoptosis related proteins, COX-2, vascular endothelial growth factor-C (VEGF-C) and lymphatic vessel density were quantified in tumor tissues by immunohistochemistry. Apoptosis was evaluated by TUNEL staining. The results revealed that celecoxib and tegafur/gimeracil/oteracil potassium alone significantly inhibited tumor growth. The combination of these two drugs showed a synergistic antitumor effect. Both celecoxib and tegafur/gimeracil/oteracil potassium alone inhibited proliferation and promoted apoptosis. The combination of these two drugs further enhanced this anticancer effect. Both celecoxib and the combination treatment inhibited lymphangiogenesis and the expression of COX-2 and VEGF-C. However, tegafur/gimeracil/oteracil potassium treatment had no obvious effect on lymphangiogenesis. These results suggested that the combination of celecoxib and tegafur/gimeracil/oteracil potassium produced a synergistic antitumor effect, possibly by inhibiting the proliferation of tumor cells and promoting apoptosis. Celecoxib and celecoxib in combination with tegafur/gimeracil/oteracil potassium possibly by reducing the expression of COX-2, in turn down-regulating the expression of VEGF-C, resulted in the inhibition of lymphangiogenesis.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCelecoxibCell Line, TumorCell ProliferationCyclooxygenase 2Drug Therapy, CombinationFemaleGastric MucosaHumansMiceMice, NudePyrazolesStomachStomach NeoplasmsAntineoplastic AgentsCelecoxibCyclooxygenase 2PyrazolesSulfonamidesVascular Endothelial Growth Factor CcelecoxibCOX-2Gastric cancerlymphangiogenesistegafur/gimeracil/oteracil potassiumVEGF-C

Identifiers

PMID25550798
PMCPMC4270618
OpenAlexW155676144

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.