Evidence map›Paper›PMID 32703317›Full record

ReviewJournal of hematology & oncology2020

Roles of hsa-miR-12462 and SLC9A1 in acute myeloid leukemia.

Yan Jia, Wei Liu, Hui-En Zhan, Xiao-Ping Yi, Hui Liang, Qi-Li Zheng, Xin-Ya Jiang, Hai-Yan Zhou, Liang Zhao, Xie-Lan Zhao and 1 more

Open access · goldAbstract readLetterReview
In one paragraph

Review in Journal of hematology & oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 22 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.

Yan JiaDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Wei LiuDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hui-En ZhanDepartment of Hematology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Xiao-Ping YiDepartment of Radiology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hui LiangDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Qi-Li ZhengDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xin-Ya JiangDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hai-Yan ZhouDepartment of Pathology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Liang ZhaoDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xie-Lan ZhaoDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hui ZengDepartment of Hematology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China. androps2011@hotmail.com.ORCID 0000-0002-4498-8888
Central South University · CNFirst Affiliated Hospital of Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) play important roles in cell proliferation, differentiation, and survival and may be useful for acute myeloid leukemia (AML) diagnosis and prognosis. In this study, we defined a novel miRNA, hsa-miR-12462, through small RNA sequencing of the bone marrow (BM) cells from 128 AML patients. Overexpression of hsa-miR-12462 in AML cells (U937 and HL-60) significantly decreased their growth rate when compared with those of the wild-type and MOCK controls. In a xenograft mouse model, tumor weight and size in the mice bearing the U937 cells with hsa-miR-12462 overexpression were significantly reduced when compared with those bearing the mock cells. The AML cells overexpressing hsa-miR-12462 had increased sensitivity to cytarabine chemotherapy. Combining the data from the MiRDB, an online microRNA database ( http://mirdb.org ), with the RNA-sequencing results, SLC9A1 was predicted to be one of the targets of hsa-miR-12462. hsa-miR-12462 was further confirmed to bind exclusively to the 3'UTR of SLC9A1 in U937 cells, leading to downregulation of SLC9A1. In summary, a higher level of hsa-miR-12462 in AML cells is associated with increased sensitivity to cytarabine chemotherapy via downregulation of SLC9A1.

Indexed as

3' Untranslated RegionsAnimalsCytarabineDrug Resistance, NeoplasmGene Expression RegulationHL-60 CellsHumansLeukemia, Myeloid, AcuteMiceNeoplasm ProteinsRNA, NeoplasmSodium-Hydrogen Exchanger 1Tumor BurdenTumor Cells, CulturedU937 CellsXenograft Model Antitumor Assays3' Untranslated RegionsCytarabineNeoplasm ProteinsRNA, NeoplasmSLC9A1 protein, humanSodium-Hydrogen Exchanger 1Acute myeloid leukemiamiRNARNA sequencingSLC9A1

Identifiers

PMID32703317
PMCPMC7376648
OpenAlexW3044845003

What OpenQuestion holds

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Registered trials

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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.