Evidence map›Paper›PMID 27137186›Full record

ReviewCellular and molecular life sciences : CMLS2016

Intestinal stem cell response to injury: lessons from Drosophila.

Huaqi Jiang, Aiguo Tian, Jin Jiang

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
–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

80 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Article
  10. Article
  11. Drosophila Intestine as a Model to Study Tumors.Advances in experimental medicine and biology · 2025
    Review
  12. Wnt/Wingless signaling promotes lipid mobilization through signal-induced transcriptional repression.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Article
  14. Bleomycin reducesMicrobiology spectrum · 2024
    Article
  15. c-Jun N-terminal kinase signaling in aging.Frontiers in aging neuroscience · 2024
    Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review

20 more citing papers are in PubMed but not listed here.

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

3 authors.

Huaqi JiangDepartment of Molecular Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 75390, USA.
Aiguo TianDepartment of Molecular Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 75390, USA.
Jin JiangDepartment of Molecular Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 75390, USA. jin.jiang@utsouthwestern.edu.

Funding

Cell signaling in development and regenerationR35GM118063 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Jin Jiang · 2016 to 2026
$9.4M
REGULATION OF HEDGEHOG SIGNALING IN DROSOPHILAR01GM061269 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI JIANG, JIN · 2000 to 2016
$4.2M
Notch signaling and fkh cooperate to maintain intestinal stem cells in DrosophilaR01DK102576 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI JIANG, HUAQI · 2015 to 2018
$1.5M
Genetic control of Drosophila intestine stem cell self-renewal and proliferationR01GM106188 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI JIANG, JIN · 2014 to 2016
$906k
NIDDK NIH HHS R01 DK102576NIGMS NIH HHS R01 GM061269NIGMS NIH HHS R01 GM106188NIGMS NIH HHS R35 GM118063
6 · The paper itself

Abstract

Many adult tissues and organs are maintained by resident stem cells that are activated in response to injury but the mechanisms that regulate stem cell activity during regeneration are still poorly understood. An emerging system to study such problem is the Drosophila adult midgut. Recent studies have identified both intrinsic factors and extrinsic niche signals that control the proliferation, self-renewal, and lineage differentiation of Drosophila adult intestinal stem cells (ISCs). These findings set up the stage to interrogate how niche signals are regulated and how they are integrated with cell-intrinsic factors to control ISC activity during normal homeostasis and regeneration. Here we review the current understanding of the mechanisms that control ISC self-renewal, proliferation, and lineage differentiation in Drosophila adult midgut with a focus on the niche signaling network that governs ISC activity in response to injury.

Indexed as

AnimalsCell DifferentiationCell LineageDrosophilaDrosophila ProteinsIntestinesJanus KinasesMicroRNAsSignal TransductionStem CellsTranscription FactorsDrosophila ProteinsJanus KinasesMicroRNAsTranscription FactorsAgingAsymmetric divisionBMPCalciumDppEGFRGbbHedgehogHhHippoInRInsulinISCJAK-STATJNKmicroRNAmidgutNNotchProliferationRasRegenerationSelf-renewalSymmetric divisionTissue damageTumorWgWntYapYki

Identifiers

PMID27137186
PMCPMC4998060

What OpenQuestion holds

Textmetadata
LicenceTDM
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.