Evidence map›Paper›PMID 36900358›Full record

ArticleCancers2023

Soluble Guanylate Cyclase β1 Subunit Represses Human Glioblastoma Growth.

Haijie Xiao, Haifeng Zhu, Oliver Bögler, Fabiola Zakia Mónica, Alexander Y Kots, Ferid Murad, Ka Bian

Open access · goldFull text read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

7 authors at 4 institutions in 2 countries.

Haijie XiaoDepartment of Biochemistry and Molecular Medicine, The George Washington University, 2300 I Street NW, Washington, DC 20037, USA.
Haifeng ZhuThe Brown Foundation Institute of Molecular Medicine for the Prevention of Human Diseases (IMM), The University of Texas Health Science Center at Houston, 7000 Fannin Street, Houston, TX 77030, USA.ORCID 0000-0001-7315-4105
Oliver BöglerBrain Tumor Center, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.
Fabiola Zakia MónicaDepartment of Biochemistry and Molecular Medicine, The George Washington University, 2300 I Street NW, Washington, DC 20037, USA.
Alexander Y KotsVeteran Affairs Palo Alto Health Care System, Department of Veteran Affairs, Palo Alto, CA 94304, USA.ORCID 0000-0002-5278-5888
Ferid MuradVeteran Affairs Palo Alto Health Care System, Department of Veteran Affairs, Palo Alto, CA 94304, USA.
Ka BianVeteran Affairs Palo Alto Health Care System, Department of Veteran Affairs, Palo Alto, CA 94304, USA.ORCID 0000-0001-6582-7787
VA Palo Alto Health Care System · USThe University of Texas MD Anderson Cancer Center · USGeorge Washington University · USUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

Role of Nitric Oxide and Cyclic GMP in Stem CellsR01GM076695 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI GORENSTEIN, DAVID G · 2007 to 2010
$1.1M
Roll of Nitrous Oxide (NO) and Cyclic GMP in CancerI01BX005709 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI BIAN, KA · 2022 to 2024
–
BLRD VA I01 BX005709NIGMS NIH HHS GM-076695-02NIGMS NIH HHS R01 GM076695
6 · The paper itself

Abstract

Malignant glioma is the most common and deadly brain tumor. A marked reduction in the levels of sGC (soluble guanylyl cyclase) transcript in the human glioma specimens has been revealed in our previous studies. In the present study, restoring the expression of sGCβ1 alone repressed the aggressive course of glioma. The antitumor effect of sGCβ1 was not associated with enzymatic activity of sGC since overexpression of sGCβ1 alone did not influence the level of cyclic GMP. Additionally, sGCβ1-induced inhibition of the growth of glioma cells was not influenced by treatment with sGC stimulators or inhibitors. The present study is the first to reveal that sGCβ1 migrated into the nucleus and interacted with the promoter of the

Indexed as

CDK6G0 arrestglioblastomaintegrin α6nucleusp53sGCβ1

Identifiers

PMID36900358
PMCPMC10001022
OpenAlexW4323044055

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read62
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.