Evidence map›Paper›PMID 35117414›Full record

ArticleTranslational cancer research2020

The expression of apolipoproteina1 and its correlation with infiltration of urologic neoplasm.

Huihui Hu, Bei Gong, Man Zhang

Open access · diamondAbstract read
In one paragraph

Article in Translational cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 65% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

3 authors at 2 institutions in 1 country.

Huihui HuDepartment of Clinical Laboratory, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Bei GongDepartment of Clinical Laboratory, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Man ZhangDepartment of Clinical Laboratory, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Capital Medical University · CNBeijing Shijitan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo explore the differential expression of apolipoproteinA1 (APOA1) in urologic neoplasm patient compared with controls, as well as investigates whether APOA1 correlated with infiltration of urologic neoplasm.

methodsA total of 59 tissue sections of surgically-resected urologic neoplasm and 6 cases of normal tissue sections were collected. Fourteen cases of urine samples from transitional cell carcinoma patients and 6 cases urine samples from controls were also applied in this experiment. We also selected 6 cases of fresh bladder transitional cell carcinoma tissues. The urologic neoplasm tissue sections were classified into infiltration and non-infiltration urologic neoplasm groups. The expressions of APOA1 between urologic neoplasm and normal control were detected by Western blot, Immunohistochemistry and qRT-PCR. The method of Immunohistochemistry was applied to examine the differences of APOA1 expression between infiltration and non-infiltration urologic neoplasm tissue section groups.

resultsCompared with none expression in normal controls, APOA1 was exhibited higher level in urologic neoplasm patient's urine and fresh bladder transitional cell carcinoma tissues (P<0.05). There were statistical differences of APOA1 between infiltration and non-infiltration urologic neoplasm tissue section groups. APOA1 expressions were found to be up-regulated in the infiltration neoplasm tissue sections compared to non-infiltration group (P<0.001).

conclusionsAPOA1 could act as a valuable biomarker for predicting the occurrence and development of urologic neoplasm.

Indexed as

ApolipoproteinA1 (APOA1)immunohistochemistryinfiltrationtissue sampleurineurologic neoplasm

Identifiers

PMID35117414
PMCPMC8798787
OpenAlexW2997706819

What OpenQuestion holds

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LicenceCC BY-NC-ND
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