Evidence map›Paper›PMID 30635654›Full record

ArticleOncogene2019

CD44s is a crucial ATG7 downstream regulator for stem-like property, invasion, and lung metastasis of human bladder cancer (BC) cells.

Junlan Zhu, Grace Huang, Xiaohui Hua, Yang Li, Huiying Yan, Xun Che, Zhongxian Tian, Huating Liufu, Chao Huang, Jingxia Li and 4 more

Abstract read
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. DNA Hydroxymethylation in Smoking-Associated Cancers.International journal of molecular sciences · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

14 authors at 2 institutions in 2 countries.

Junlan ZhuNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Grace HuangNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Xiaohui HuaNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Yang LiNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Huiying YanZhejiang Provincial Key Laboratory for Technology and Application of Model Organisms, Key Laboratory of Laboratory Medicine, Ministry of Education, China, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Xun CheNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Zhongxian TianNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Huating LiufuNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Chao HuangNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Jingxia LiNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Jiheng XuNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Wei DaiNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA.
Haishan HuangZhejiang Provincial Key Laboratory for Technology and Application of Model Organisms, Key Laboratory of Laboratory Medicine, Ministry of Education, China, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China. haishan_333@163.com.
Chuanshu HuangNelson Institute of Environmental Medicine, New York University School of Medicine, New York, NY, 10010, USA. Chuanshu.huang@nyulangone.org.
New York University · USWenzhou Medical University · CN

Funding

RESEARCH IN ENVIRONMENTAL HEALTH SCIENCES (CENTER GRANT)P30ES000260 · NIEHS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI COSTA, MAX · 1985 to 2020
$26.1M
Reagent/Service CoreP01CA165980 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WU, XUE-RU · 2013 to 2023
$13.5M
SESN2 and therapeutic effect of Isohapontigenin (ISO)R01CA217923 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI COSTA, MAX, SUN, HONG · 2018 to 2022
$2.1M
Mechanisms underlying therapeutic effect of a new compound Isorhapontigenin (ISO)R01CA177665 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HUANG, CHUANSHU · 2013 to 2018
$1.7M
NCI NIH HHS P01 CA165980NCI NIH HHS R01 CA177665NCI NIH HHS R01 CA217923NIEHS NIH HHS P30 ES000260U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) CA165980U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) CA177665U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) CA217923U.S. Department of Health & Human Services | NIH | National Institute of Environmental Health Sciences (NIEHS) ES000260
6 · The paper itself

Abstract

Over half a million US residents are suffering with bladder cancer (BC), which costs a total $4 billion in treatment annually. Although recent studies report that autophagy-related gene 7 (ATG7) is overexpressed in BCs, the regulatory effects of ATG7 on cancer stem-like phenotypes and invasion have not been explored yet. Current studies demonstrated that the deficiency of ATG7 by its shRNA dramatically reduced sphere formation and invasion in vitro, as well as lung metastasis in vivo in human invasive BC cells. Further studies indicated that the knockdown of ATG7 attenuated the expression of CD44 standard (CD44s), while ectopic introduction of CD44s, was capable of completely restoring sphere formation, invasion, and lung metastasis in T24T(shATG7) cells. Mechanistic studies revealed that ATG7 overexpression stabilized CD44s proteins accompanied with upregulating USP28 proteins. Upregulated USP28 was able to bind to CD44s and remove the ubiquitin group from CD44s' protein, resulting in the stabilization of CD44s protein. Moreover, ATG7 inhibition stabilized AUF1 protein and thereby reduced tet1 mRNA stability and expression, which was able to demethylate usp28 promoter, reduced USP28 expression, finally promoting CD44s degradation. In addition, CD44s was defined to inhibit degradation of RhoGDIβ, which in turn promotes BC invasion. Our results demonstrate that CD44s is a key ATG7 downstream regulator of the sphere formation, invasion, and lung metastasis of BCs, providing significant insight into understanding the BC invasions, metastasis, and stem-like properties.

Indexed as

Autophagy-Related Protein 7Cell Line, TumorHumansHyaluronan ReceptorsLung NeoplasmsMixed Function OxygenasesNeoplasm MetastasisPromoter Regions, GeneticRNA, Small InterferingUbiquitin ThiolesteraseUp-RegulationUrinary Bladder NeoplasmsATG7 protein, humanAutophagy-Related Protein 7CD44 protein, humanHyaluronan ReceptorsMixed Function OxygenasesRNA, Small InterferingUbiquitin Thiolesterase

Identifiers

PMID30635654
PMCPMC7112719
OpenAlexW2909320299

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.