Evidence map›Paper›PMID 29725424›Full record

ArticleOncology letters2018

Overexpression of ATP citrate lyase in renal cell carcinoma tissues and its effect on the human renal carcinoma cells

Lichen Teng, Yongsheng Chen, Yan Cao, Wentao Wang, Yongpeng Xu, Yanjie Wang, Jiayin Lv, Changfu Li, Yajuan Su

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
1.9field-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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

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  14. Lipid metabolism reprogramming in renal cell carcinomas.Medical oncology (Northwood, London, England) · 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.

Lichen TengDepartment of Urology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150080, P.R. China.
Yongsheng ChenDepartment of Urology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150080, P.R. China.
Yan CaoDepartment of Urology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150080, P.R. China.
Wentao WangDepartment of Urology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150080, P.R. China.
Yongpeng XuDepartment of Urology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150080, P.R. China.
Yanjie WangDepartment of Urology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150080, P.R. China.
Jiayin LvDepartment of Urology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150080, P.R. China.
Changfu LiDepartment of Urology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150080, P.R. China.
Yajuan SuDepartment of Laboratory, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150080, P.R. China.
Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ATP citrate lyase (ACLY) is a key enzyme of lipogenesis in cells. However, ACLY expression in renal cell carcinoma (RCC) and its association with clinicopathological parameters remain unclear. The present study aimed to evaluate ACLY expression levels in RCC and adjacent normal tissues. This study included 33 patients with clear cell RCC (ccRCC). ACLY protein was assayed using immunohistochemistry and western blotting methods. ACLY mRNA expression was determined by reverse transcription-quantitative polymerase chain reaction. Serum ACLY concentrations were measured using the ELISA. Compared with adjacent normal tissues, significantly higher levels of ACLY protein expression were observed in all of the ccRCC tissues (P<0.05). ACLY protein levels were positively associated with the T stage and nuclear grade of RCC. ACLY immunostaining was located in the cytoplasm and nucleus. ACLY protein levels and ACC1 mRNA expression in RCC tissues were significantly higher compared with that in adjacent normal tissues (P<0.05). There were no significant differences in serum ACLY concentrations between patients with RCC and health controls (P>0.05). Preliminary evaluation of ACLY function showed that ACLY small interfering RNA downregulation inhibited RCC cell proliferation and migration, but promoted RCC cell apoptosis. ACLY may be a novel biomarker for the evaluation of biological aggressiveness and may be a potential target for RCC treatment.

Indexed as

ATP citrate lyaselipogenesismetabolicrenal cell carcinoma

Identifiers

PMID29725424
PMCPMC5920499
OpenAlexW2793895466

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.