Evidence map›Paper›PMID 27819521›Full record

ArticleCancer biology & therapy2018

MicroRNA-326 sensitizes human glioblastoma cells to curcumin via the SHH/GLI1 signaling pathway.

Shi Yin, Wenzhong Du, Feng Wang, Bo Han, Yuqiong Cui, Dongbo Yang, Hui Chen, Daming Liu, Xing Liu, Xiuwei Zhai and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer biology & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.4field-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

28 citing papers in PubMed, 55 citations in OpenAlex.

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  4. The Small Molecules of Plant Origin with Anti-Glioma Activity.International journal of molecular sciences · 2025
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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.

Shi Yina Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Wenzhong Dua Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Feng Wanga Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Bo Hana Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Yuqiong Cuia Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Dongbo Yanga Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Hui Chena Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Daming Liua Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Xing Liua Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Xiuwei Zhaic Department of Neurosurgery , Daqing LongNan Hospital , Daqing , China.
Chuanlu Jianga Department of Neurosurgery , The Second Affiliated Hospital of Harbin Medical University , Harbin , China.
Harbin Medical University · CNSecond Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme is the most malignant and common brain tumor in adults and is characterized by poor survival and high resistance to chemotherapy and radiotherapy. Among the new chemotherapy drugs, curcumin, a popular dietary supplement, has proven to have a potent anticancer effect on a variety of cancer cell types; however, it remains difficult to achieve a satisfactory therapeutic effect with curcumin using the traditional single-drug treatment. In this study, we found that expression of miR-326, a tumor suppressor microRNA in various tumor types, resulted in a marked increase of curcumin-induced cytotoxicity and apoptosis and a decrease of proliferation and migration in glioma cells. Moreover, we found that combination treatment of miR-326 and curcumin caused significant inhibition of the SHH/GLI1 pathway in glioma cells compared with either treatment alone, independent of p53 status. Furthermore, in vivo, the curcumin-induced increase in miR-326 expression altered the anti-glioma mechanism of this combination treatment, which further reduced tumor volume and prolonged the survival period compared to either treatment alone. Taken together, our data strongly support an important role for miR-326 in enhancing the chemosensitivity of glioma cells to curcumin.

Indexed as

AdultAntineoplastic AgentsApoptosisBrain NeoplasmsCell Line, TumorCell ProliferationCurcuminDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticGlioblastomaHedgehog ProteinsHumansMicroRNAsSignal TransductionZinc Finger Protein GLI1Antineoplastic AgentsCurcuminGLI1 protein, humanHedgehog ProteinsMicroRNAsMIRN326 microRNA, humanSHH protein, humanZinc Finger Protein GLI1CurcuminGLI1gliomaMicroRNAp53tumor

Identifiers

PMID27819521
PMCPMC5902238
OpenAlexW2555757312

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.