Evidence map›Paper›PMID 25268611›Full record

ArticleInternational journal of molecular sciences2014

Gender-associated genomic differences in colorectal cancer: clinical insight from feminization of male cancer cells.

Rola H Ali, Makia J Marafie, Milad S Bitar, Fahad Al-Dousari, Samar Ismael, Hussain Bin Haider, Waleed Al-Ali, Sindhu P Jacob, Fahd Al-Mulla

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Sex differences in disease: sex chromosome and immunity.Journal of translational medicine · 2024
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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 at 2 institutions in 1 country.

Rola H AliDepartment of Pathology, Faculty of Medicine, Health Sciences Center, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait. rolapath@hotmail.com.
Makia J MarafieKuwait Medical Genetics Center, Ministry of Health, Safat 13001, Kuwait. mj_marafie@yahoo.com.
Milad S BitarDepartment of Pharmacology, Faculty of Medicine, Health Sciences Center, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait. milad.bitar@gmail.com.
Fahad Al-DousariDepartment of Forensic Evidence, Ministry of Interior, P.O. Box 12500, Shamiya 71655, Kuwait. fahad77@hotmail.com.
Samar IsmaelDepartment of Forensic Evidence, Ministry of Interior, P.O. Box 12500, Shamiya 71655, Kuwait. sismaeel@yahoo.com.
Hussain Bin HaiderDepartment of Pathology, Faculty of Medicine, Health Sciences Center, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait. hus4in@live.com.
Waleed Al-AliDepartment of Pathology, Faculty of Medicine, Health Sciences Center, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait. waleed_mls@hotmail.com.
Sindhu P JacobDepartment of Pathology, Faculty of Medicine, Health Sciences Center, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait. sindhujacob@hsc.edu.kw.
Fahd Al-MullaDepartment of Pathology, Faculty of Medicine, Health Sciences Center, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait. fahd@al-mulla.org.
Kuwait University · KWMinistry of Health · KW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gender-related differences in colorectal cancer (CRC) are not fully understood. Recent studies have shown that CRC arising in females are significantly associated with CpG island methylator phenotype (CIMP-high). Using array comparative genomic hybridization, we analyzed a cohort of 116 CRCs (57 males, 59 females) for chromosomal copy number aberrations (CNA) and found that CRC in females had significantly higher numbers of gains involving chromosome arms 1q21.2-q21.3, 4q13.2, 6p21.1 and 16p11.2 and copy number losses of chromosome arm 11q25 compared to males. Interestingly, a subset of male CRCs (46%) exhibited a "feminization" phenomenon in the form of gains of X chromosomes (or an arm of X) and/or losses of the Y chromosome. Feminization of cancer cells was significantly associated with microsatellite-stable CRCs (p-value 0.003) and wild-type BRAF gene status (p-value 0.009). No significant association with other clinicopathological parameters was identified including disease-free survival. In summary, our data show that some CNAs in CRC may be gender specific and that male cancers characterized by feminization may constitute a specific subset of CRCs that warrants further investigation.

Indexed as

Genome, HumanAdultAgedAged, 80 and overChromosomes, Human, XChromosomes, Human, YColorectal NeoplasmsComparative Genomic HybridizationDemographyDisease-Free SurvivalDNA Copy Number VariationsFemaleFeminizationHumansIn Situ Hybridization, FluorescenceMaleProto-Oncogene Proteins B-raf

Identifiers

PMID25268611
PMCPMC4227166
OpenAlexW2105789311

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.