Evidence map›Paper›PMID 32270028›Full record

ArticleAdvanced biosystems2019

Senescent Cells with Augmented Cytokine Production for Microvascular Bioengineering and Tissue Repairs.

Yang Xiao, Chang Liu, Zhuo Chen, Michael R Blatchley, Dongjoo Kim, Jing Zhou, Ming Xu, Sharon Gerecht, Rong Fan

Abstract read
In one paragraph

Article in Advanced biosystems, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Skin Aging, Cellular Senescence and Natural Polyphenols.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. 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

9 authors.

Yang XiaoDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, U.S.A.
Chang LiuDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, U.S.A.
Zhuo ChenDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, U.S.A.
Michael R BlatchleyDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 20218, U.S.A.
Dongjoo KimDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, U.S.A.
Jing ZhouDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, U.S.A.
Ming XuDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, U.S.A.
Sharon GerechtDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 20218, U.S.A.
Rong FanDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, U.S.A.

Funding

Project 3: Single Cell Measures of Intratumor Diversity for Optimal Breast Cancer TherapyU54CA193461 · NCI · DANA-FARBER CANCER INST · PI MICHOR, FRANZISKA · 2015 to 2020
$11.2M
Systems analysis of phenotypic switch in control of cancer invasionU54CA209992 · NCI · YALE UNIVERSITY · PI LEVCHENKO, ANDRE · 2016 to 2021
$10.1M
The Role of Physical Cues in Collective Cell InvasionU54CA210173 · NCI · JOHNS HOPKINS UNIVERSITY · PI PIENTA, KENNETH J., WIRTZ, DENIS · 2016 to 2020
$9.9M
Yale Cooperative Hematology Specialized Core CenterU54DK106857 · NIDDK · YALE UNIVERSITY · PI JOHN HWA, Diane S Krause · 2015 to 2026
$9.7M
T32: Predoctoral and Postdoctoral Training Program in Nanotechnology for Cancer ResearchT32CA153952 · NCI · JOHNS HOPKINS UNIVERSITY · PI Denis Wirtz · 2015 to 2026
$3.5M
T-32 NIH Postdoctoral Training Program in Nanotechnology for Cancer Medicine NTCMT32CA130840 · NCI · JOHNS HOPKINS UNIVERSITY · PI WIRTZ, DENIS · 2008 to 2012
$1.2M
Elucidating a mechanism for hypoxic cluster-based vasculogenesisF31HL137339 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BLATCHLEY, MICHAEL · 2017 to 2019
$93k
NCI NIH HHS T32 CA130840NCI NIH HHS T32 CA153952NCI NIH HHS U54 CA193461NCI NIH HHS U54 CA209992NCI NIH HHS U54 CA210173NHLBI NIH HHS F31 HL137339NIDDK NIH HHS U54 DK106857
6 · The paper itself

Abstract

Controlled delivery of cytokines and growth factors has been an area of intense research interest for molecular and cellular bioengineering, immunotherapy, and regenerative medicine. In this study, we show that primary human lung fibroblasts chemically induced to senescence (cell cycle arrest) can act as a living source to transiently produce factors essential for promoting vasculogenesis or angiogenesis, such as VEGF, HGF, and IL-8. Co-culture of senescent fibroblasts with HUVECs in a fibrin gel demonstrated accelerated formation and maturation of microvessel networks in as early as three days. Unlike the usage of non-senescent fibroblasts as the angiogenesis-promoting cells, this approach eliminates drawbacks related to the overproliferation of fibroblasts and the subsequent disruption of tissue architecture, integrity, or function. Co-culture of pancreatic islets with senescent fibroblasts and endothelial cells in a gel matrix maintains the viability and function of islets

Indexed as

cytokinesmicrovasculaturesenescent cellstissue engineering

Identifiers

PMID32270028
PMCPMC7141414

What OpenQuestion holds

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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.