Evidence map›Paper›PMID 35831364›Full record

ArticleScientific reports2022

Transgenic overexpression of microRNA-30d in pancreatic beta-cells progressively regulates beta-cell function and identity.

Yiping Mao, Jacob Schoenborn, Zhihong Wang, Xinqian Chen, Katy Matson, Ramkumar Mohan, Shungang Zhang, Xiaohu Tang, Anoop Arunagiri, Peter Arvan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 7 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.

Yiping MaoDepartment of Biological Sciences, Michigan Technological University, Houghton, MI, 49931, USA.
Jacob SchoenbornDepartment of Biological Sciences, Michigan Technological University, Houghton, MI, 49931, USA.
Zhihong WangDepartment of Biological Sciences, Michigan Technological University, Houghton, MI, 49931, USA.
Xinqian ChenDepartment of Biological Sciences, Michigan Technological University, Houghton, MI, 49931, USA.
Katy MatsonDepartment of Biological Sciences, Michigan Technological University, Houghton, MI, 49931, USA.
Ramkumar MohanDepartment of Biological Sciences, Michigan Technological University, Houghton, MI, 49931, USA.
Shungang ZhangDepartment of Biological Sciences, Michigan Technological University, Houghton, MI, 49931, USA.
Xiaohu TangDepartment of Biological Sciences, Michigan Technological University, Houghton, MI, 49931, USA.
Anoop ArunagiriDepartment of Metabolism Endocrinology and Diabetes, University of Michigan, Ann Arbor, MI, 48109, USA.
Peter ArvanDepartment of Metabolism Endocrinology and Diabetes, University of Michigan, Ann Arbor, MI, 48109, USA.
Xiaoqing TangDepartment of Biological Sciences, Michigan Technological University, Houghton, MI, 49931, USA. xtang2@mtu.edu.
Michigan Technological University · USUniversity of Michigan–Ann Arbor · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Proinsulin Trafficking for Insulin BiosynthesisR01DK048280 · NIDDK · YESHIVA UNIVERSITY · PI ARVAN, PETER · 1994 to 2024
$10.5M
Role of miR-483 in Pancreatic Alpha and Beta CellsR15DK103197 · NIDDK · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI TANG, XIAOQING · 2015 to 2015
$422k
Exploiting synthetic lethality of cysteine addiction to target breast cancerR15CA246336 · NCI · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI TANG, XIAOHU · 2020 to 2020
$413k
Role of miR-30d in insulin gene expression in pancreatic beta cellsR03DK084166 · NIDDK · UNIVERSITY OF KENTUCKY · PI TANG, XIAOQING · 2009 to 2010
$150k
NCI NIH HHS R15 CA246336NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK048280NIDDK NIH HHS R03 DK084166NIDDK NIH HHS R15 DK103197NIH HHS CA246336NIH HHS DK084166, DK103197NIH HHS DK48280
6 · The paper itself

Abstract

Abnormal microRNA functions are closely associated with pancreatic β-cell loss and dysfunction in type 2 diabetes. Dysregulation of miR-30d has been reported in the individuals with diabetes. To study how miR-30d affects pancreatic β-cell functions, we generated two transgenic mouse lines that specifically overexpressed miR-30d in β-cells at distinct low and high levels. Transgenic overexpressed miR-30d systemically affected β-cell function. Elevated miR-30d at low-level (TgL, 2-fold) had mild effects on signaling pathways and displayed no significant changes to metabolic homeostasis. In contrast, transgenic mice with high-level of miR-30d expression (TgH, 12-fold) exhibited significant diet-induced hyperglycemia and β-cell dysfunction. In addition, loss of β-cell identity was invariably accompanied with increased insulin/glucagon-double positive bihormonal cells and excess plasma glucagon levels. The transcriptomic analysis revealed that miR-30d overexpression inhibited β-cell-enriched gene expression and induced α-cell-enriched gene expression. These findings implicate that an appropriate miR-30d level is essential in maintaining normal β-cell identity and function.

Indexed as

Diabetes Mellitus, Type 2Glucagon-Secreting CellsInsulin-Secreting CellsMicroRNAsAnimalsGlucagonMiceGlucagonMicroRNAsMirn30d microRNA, mouse

Identifiers

PMID35831364
PMCPMC9279310
OpenAlexW4285393277

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.