Evidence map›Paper›PMID 26464702›Full record

ArticleInternational journal of clinical and experimental pathology2015

Immunohistochemistry of p53 and Ki-67 and p53 mutation analysis in renal epithelioid angiomyolipoma.

Wenbin Li, Lei Guo, Xingang Bi, Jianhui Ma, Shan Zheng

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. 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
1.7field-weighted citation impact, top 15% 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, 20 citations in OpenAlex.

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  12. The Risks of Renal Angiomyolipoma: Reviewing the Evidence.Journal of kidney cancer and VHL · 2017
    Review
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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 1 institution in 1 country.

Wenbin LiDepartment of Pathology, Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College Beijing 100021, China.
Lei GuoDepartment of Pathology, Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College Beijing 100021, China.
Xingang BiDepartment of Urology, Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College Beijing 100021, China.
Jianhui MaDepartment of Urology, Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College Beijing 100021, China.
Shan ZhengDepartment of Pathology, Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College Beijing 100021, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgoundRenal epithelioid angiomyolipoma (EAML) is a rare variant of AML (angiomyolipoma) and is often associated with aggressive behaviors. The pathogenesis of EAML has been poorly understood. We analyzed the expression of p53 and Ki-67 by immunohistochemistry (IHC) and investigated p53 mutation analysis in 11 cases of EAML in comparison to classical AML.

methodsP53 and Ki-67 expression status were determined by IHC staining. P53 mutation analysis was performed using bi-directional sequencing.

resultsRenal EAML tumors were significantly associated with more severe to moderate nuclear atypia (100% vs. 36.4%, P = 0.004) and mitotic activity (90.9% vs. 27.3%, P = 0.008) compared with AML tumors. Out of 11 cases of EAML, 8 were positive for p53. There was only 1 case with positive p53 expression in AML cases and expression of p53 protein showed significant difference between EAML and AML tumors (72.7% vs. 9.1%, P = 0.008). In addition, there were 7 AML and 6 EAML cases harbored P72R mutation (SNP) in exon 4 of p53. Compared with AML cases, 2 out of 11 cases of EMAL showed more than 10% positivity for ki-67. The finding of stronger p53 expression in renal EAML might have contributed to their malignant behavior. However, the abnormal p53 expression cannot be entirely explained by p53 mutations in the exons examined.

conclusionsThus, the combination of immunohistochemical assessment of tumor antigens might improve our ability to predict the malignant outcome in EAML.

Indexed as

MutationAdultAngiomyolipomaDNA Mutational AnalysisEpithelioid CellsFemaleHumansImmunohistochemistryKi-67 AntigenKidney NeoplasmsMaleMiddle AgedTumor Suppressor Protein p53Ki-67 AntigenTumor Suppressor Protein p53EAMLimmunohistochemistryKi-67mutation analysisp53

Identifiers

PMID26464702
PMCPMC4583934
OpenAlexW2396640347

What OpenQuestion holds

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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.