Evidence map›Paper›PMID 30744076›Full record

ArticleCancers2019

Identification of Cross Talk between FoxM1 and RASSF1A as a Therapeutic Target of Colon Cancer.

Thomas G Blanchard, Steven J Czinn, Vivekjyoti Banerjee, Neha Sharda, Andrea C Bafford, Fahad Mubariz, Dennis Morozov, Antonino Passaniti, Hafiz Ahmed, Aditi Banerjee

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Organoid of ovarian cancer: genomic analysis and drug screening.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Review
  6. Article
  7. Review
  8. 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

10 authors at 1 institution in 1 country.

Thomas G BlanchardDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, MD 21201, USA. tblanchard@som.umaryland.edu.
Steven J CzinnDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, MD 21201, USA. SCzinn@som.umaryland.edu.
Vivekjyoti BanerjeeDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, MD 21201, USA. vivekjyoti24@gmail.com.
Neha ShardaDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, MD 21201, USA. nehasharda4@gmail.com.
Andrea C BaffordDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA. ABafford@som.umaryland.edu.
Fahad MubarizDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, MD 21201, USA. fahad.mubariz@umaryland.edu.
Dennis MorozovDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, MD 21201, USA. dennismorozov98@gmail.com.
Antonino PassanitiDepartment of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201, USA. TPassaniti@som.umaryland.edu.
Hafiz AhmedGlycoMantra Inc, Baltimore, MD 21227, USA. hfzahmed86@gmail.com.
Aditi BanerjeeDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, MD 21201, USA. aditi.banerjee@som.umaryland.edu.
University of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastatic colorectal cancer (mCRC) is characterized by the expression of cellular oncogenes, the loss of tumor suppressor gene function. Therefore, identifying integrated signaling between onco-suppressor genes may facilitate the development of effective therapy for mCRC. To investigate these pathways we utilized cell lines and patient derived organoid models for analysis of gene/protein expression, gene silencing, overexpression, and immunohistochemical analyses. An inverse relationship in expression of oncogenic FoxM1 and tumor suppressor RASSF1A was observed in various stages of CRC. This inverse correlation was also observed in mCRC cells lines (T84, Colo 205) treated with Akt inhibitor. Inhibition of FoxM1 expression in mCRC cells as well as in our ex vivo model resulted in increased RASSF1A expression. Reduced levels of RASSF1A expression were found in normal cells (RWPE-1, HBEpc, MCF10A, EC) stimulated with exogenous VEGF

Indexed as

cancer organoidsFoxM1metastatic colon cancer (mCRC)p-YAPRASSF1A

Identifiers

PMID30744076
PMCPMC6406751
OpenAlexW2911874207

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.