Evidence map›Paper›PMID 30665445›Full record

ArticleJournal of experimental & clinical cancer research : CR2019

miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2.

Ying Zhang, Fan Xia, Fan Zhang, Yingying Cui, Qingling Wang, Hui Liu, Yongping Wu

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

44 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. miRNAs as short non-coding RNAs in regulating doxorubicin resistance.Journal of cell communication and signaling · 2023
    Review
  12. Landscape of NcRNAs involved in drug resistance of breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Oncology letters · 2022
    Article
  19. Article
  20. The Role of MiRNA in Cancer: Pathogenesis, Diagnosis, and Treatment.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
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.

Ying ZhangDepartment of Pathology, Laboratory of Clinical and Experimental Pathology, Xuzhou Medical University, No. 209, Tongshan Rd, Xuzhou, 221004, China.
Fan XiaKey Laboratory of Bone Marrow Stem Cell of Jiangsu Province, Xuzhou Medical University, No. 84, Huaihaixi Rd, Xuzhou, 221002, China.
Fan ZhangKey Laboratory of Bone Marrow Stem Cell of Jiangsu Province, Xuzhou Medical University, No. 84, Huaihaixi Rd, Xuzhou, 221002, China.
Yingying CuiDepartment of Pathology, The Affiliated Hospital of Xuzhou Medical University, No. 99, Huaihaixi Rd, Xuzhou, 221002, China.
Qingling WangDepartment of Pathology, Laboratory of Clinical and Experimental Pathology, Xuzhou Medical University, No. 209, Tongshan Rd, Xuzhou, 221004, China.
Hui LiuDepartment of Pathology, The Affiliated Hospital of Xuzhou Medical University, No. 99, Huaihaixi Rd, Xuzhou, 221002, China.
Yongping WuDepartment of Pathology, Laboratory of Clinical and Experimental Pathology, Xuzhou Medical University, No. 209, Tongshan Rd, Xuzhou, 221004, China. wyp@xzhmu.edu.cn.

Funding

National Natural Science Foundation of China 81372479National Natural Science Foundation of China 81671584
6 · The paper itself

Abstract

backgroundThe pro-oncogenic anterior gradient 2 (AGR2) is involved in tumor growth and drug resistance of breast cancer. Mechanisms that regulate expression of AGR2 still need to be elucidated.

methodsIn this study, expression levels of AGR2 and miR-135b-5p were analyzed in different breast cancer cell lines as well as in clinical breast cancer tissues. The in vitro and in vivo functional effect of AGR2 and miR-135b-5p were also investigated. A luciferase reporter assay was applied to confirm the interaction between miR-135b-5p and AGR2 mRNA.

resultsWe identified AGR2 as a target of miR-135b-5p. Expression of AGR2 was up-regulated in doxorubicin-resistant breast cancer cells. AGR2 mediated doxorubicin-sensitivity of breast cancer cells both in vitro and in vivo. miR-135b-5p negatively regulated AGR2-expression of breast cancer cells increasing doxorubicin-sensitivity. However, miR-135b-5p was down-regulated in doxorubicin-resistant breast cancer cells as well as during treatment with doxorubicin, which might be a probable reason for over-expression of AGR2. Up-regulation of miR-135b-5p increased doxorubicin-sensitivity of breast cancer cells in vivo. In addition, levels of AGR2 negatively correlated with levels of miR-135b-5p in clinical breast cancer tissue samples.

conclusionOur results highlight the potential of miR-135b-5p as a target for treating AGR2-expressing breast cancer with doxorubicin-resistance.

Indexed as

Breast NeoplasmsCell ProliferationDoxorubicinDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticHumansMCF-7 CellsMicroRNAsMucoproteinsOncogene ProteinsProteinsSignal TransductionAGR2 protein, humanDoxorubicinMicroRNAsMIRN135 microRNA, humanMucoproteinsOncogene ProteinsProteinsAnterior gradient 2Breast cancerDoxorubicinmicroRNA

Identifiers

PMID30665445
PMCPMC6341729

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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.