Evidence map›Paper›PMID 24649208›Full record

ArticleMolecular and clinical oncology2013

Peroxiredoxin V: A candidate breast tumor marker of population specificity.

Amany Elamin, Hongxia Zhu, A M El Hassan, Ningzhi Xu, Muntasir E Ibrahim

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and clinical oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

Amany ElaminDepartment of Molecular Biology, Institute of Endemic Diseases, University of Khartoum, Khartoum 11111, Sudan ;
Hongxia ZhuLaboratory of Cell and Molecular Biology, Cancer Institute and Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, P.R. China ;
A M El HassanDepartment of Molecular Biology, Institute of Endemic Diseases, University of Khartoum, Khartoum 11111, Sudan ;
Ningzhi XuLaboratory of Cell and Molecular Biology, Cancer Institute and Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, P.R. China ;
Muntasir E IbrahimDepartment of Molecular Biology, Institute of Endemic Diseases, University of Khartoum, Khartoum 11111, Sudan ;
University of Khartoum · SDChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast and cervical cancers account for approximately 50% of all types of cancer in Sudanese women. In a previous preliminary proteomic study aimed to identify proteins that were differentially expressed between tumors and control tissues (n=24), we identified peroxiredoxin V (PrdxV) as a candidate tumor marker. Peroxiredoxins (Prdxs) are a family of multifunctional proteins that are involved in the cell protection against oxidative stress, modulation of intracellular signaling, and regulation of cell proliferation. Knockout animal models suggest that the regulation of these proteins may be a novel target for therapeutic interventions. A total of 91 tumors and 79 normal breast tissues obtained from a panel of 106 Sudanese breast cancer patients, as well as 31 paired tissue samples (tumors and controls) from Chinese cancer patients were included in this study. Tissue sections were examined using immunohistochemistry (IHC) for PrdxI, V and VI antibodies. The PrdxV mRNA pattern of expression was also investigated using

Indexed as

breast cancerperoxiredoxinspost-translational modificationstumor marker

Identifiers

PMID24649208
PMCPMC3915645
OpenAlexW2071078609

What OpenQuestion holds

Textmetadata
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.