Evidence map›Paper›PMID 25400759›Full record

ArticleInternational journal of clinical and experimental pathology2014

MiR-634 sensitizes nasopharyngeal carcinoma cells to paclitaxel and inhibits cell growth both in vitro and in vivo.

Xiaowei Peng, Peiguo Cao, Dong He, Shuang Han, Jianda Zhou, Guolin Tan, Wei Li, Fenghui Yu, Jianjun Yu, Zan Li and 1 more

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. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.2field-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

21 citing papers in PubMed, 29 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

11 authors at 2 institutions in 1 country.

Xiaowei PengDepartment of Head and Neck Surgery, The Affiliated Cancer Hospital of Xiangya Medical School, Central South University Changsha 410013, Hunan, China.
Peiguo CaoDepartment of Oncology, The Third Xiangya Hospital, Central South University Changsha 410013, Hunan, China.
Dong HeDepartment of Respiratory, The Second People's Hospital of Hunan Province Changsha 410013, Hunan, China.
Shuang HanDepartment of Oncology, The Third Xiangya Hospital, Central South University Changsha 410013, Hunan, China.
Jianda ZhouDepartment of Plastic Surgery, The Third Xiangya Hospital, Central South University Changsha 410013, Hunan, China.
Guolin TanDepartment of Otolaryngology-Head and Neck Surgery, The Third Xiangya Hospital, Central South University Changsha 410013, Hunan, China.
Wei LiDepartment of Otolaryngology-Head and Neck Surgery, The Third Xiangya Hospital, Central South University Changsha 410013, Hunan, China.
Fenghui YuDepartment of Head and Neck Surgery, The Affiliated Cancer Hospital of Xiangya Medical School, Central South University Changsha 410013, Hunan, China.
Jianjun YuDepartment of Head and Neck Surgery, The Affiliated Cancer Hospital of Xiangya Medical School, Central South University Changsha 410013, Hunan, China.
Zan LiDepartment of Head and Neck Surgery, The Affiliated Cancer Hospital of Xiangya Medical School, Central South University Changsha 410013, Hunan, China.
Ke CaoDepartment of Oncology, The Third Xiangya Hospital, Central South University Changsha 410013, Hunan, China.
Central South University · CNSecond People Hospital of Hunan · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resistance to chemotherapy is one of the key causal factors in cancer death and increasing evidence has revealed that microRNAs (miRNAs) are involved in chemoresistance in many kinds of human cancers. Paclitaxel has been used for treatment of advanced nasopharyngeal carcinoma (NPC); however, treatment failure often occurs due to development of acquired paclitaxel resistance. In this study, based on miRNA microarray screening and qRT-PCR validation, we found six differentially expressed miRNAs in our induced paclitaxel-resistant NPC CNE-1/Taxol cells. Furthermore, we clarified the role of miR-634, most significantly downregulated in the paclitaxel-resistant CNE-1/Taxol, in regulating the paclitaxel sensitivity in NPC cells. We restored miR-634 expression in the CNE-1/Taxol cells by lentivirus infection, and found restoration of miR-634 re-sensitized the CNE-1/Taxol cells to paclitaxel in vitro by MTT assay and colony formation assay. In xenograft mouse model, we found that miR-634 inhibited tumor growth and enhanced paclitaxel sensitivity. Thus, our findings provide important information for the development of targeted gene therapy for reversing paclitaxel resistance in NPC.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicCarcinomaCell Line, TumorCell ProliferationDose-Response Relationship, DrugDrug Resistance, NeoplasmFemaleGene Expression ProfilingHumansMice, NudeMicroRNAsNasopharyngeal CarcinomaNasopharyngeal NeoplasmsOligonucleotide Array Sequence AnalysisPaclitaxelAntineoplastic Agents, PhytogenicMicroRNAsMIRN-634 microRNA, humanPaclitaxelMicroarraynasopharyngeal carcinomapaclitaxel resistancetargeted therapy

Identifiers

PMID25400759
PMCPMC4230079
OpenAlexW1937166149

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.