Evidence map›Paper›PMID 28494778›Full record

ArticleJournal of experimental & clinical cancer research : CR2017

Lysophosphatidylcholine acyltransferase 1 upregulation and concomitant phospholipid alterations in clear cell renal cell carcinoma.

Yiqing Du, Qiang Wang, Xingzhong Zhang, Xiaofeng Wang, Caipeng Qin, Zhengzuo Sheng, Huaqi Yin, Changtao Jiang, Jing Li, Tao Xu

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

60 citing papers in PubMed, 101 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

10 authors at 2 institutions in 1 country.

Yiqing DuDepartment of Urology, Peking University People's Hospital, No. 11 Xi Zhi Men South Street, Beijing, 100044, China.
Qiang WangDepartment of Urology, Peking University People's Hospital, No. 11 Xi Zhi Men South Street, Beijing, 100044, China.
Xingzhong ZhangDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Key Cardiovascular Science, Ministry of Education and Beijing Key Laboratory of Cardiovascular Receptors Research, Beijing, China.
Xiaofeng WangDepartment of Urology, Peking University People's Hospital, No. 11 Xi Zhi Men South Street, Beijing, 100044, China.
Caipeng QinDepartment of Urology, Peking University International Hospital, Beijing, China.
Zhengzuo ShengDepartment of Urology, Peking University People's Hospital, No. 11 Xi Zhi Men South Street, Beijing, 100044, China.
Huaqi YinDepartment of Urology, Peking University People's Hospital, No. 11 Xi Zhi Men South Street, Beijing, 100044, China.
Changtao JiangDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Key Cardiovascular Science, Ministry of Education and Beijing Key Laboratory of Cardiovascular Receptors Research, Beijing, China.
Jing LiDepartment of Gastroenterology, Peking University People's Hospital, No. 11 Xi Zhi Men South Street, Beijing, 100044, China. s-a-sally@163.com.
Tao XuDepartment of Urology, Peking University People's Hospital, No. 11 Xi Zhi Men South Street, Beijing, 100044, China. xutao@pkuph.edu.cn.
Peking University · CNPeking University People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe involvement of lipid metabolism in tumourigenesis and the progression of clear cell renal cell carcinoma (ccRCC) have been reported. However, the role of phospholipid profile alterations in ccRCC has not yet been systematically explored. In the present study, we compared the phospholipid compositions between ccRCC and paired normal renal tissues.

methodsThe phospholipid compositions of paired ccRCC and normal renal tissues were evaluated using liquid chromatography tandem mass spectrometry (LC/MS/MS). To evaluate the mRNA and protein levels of lysophosphatidylcholine acyltransferase (LPCAT), which converts lysophosphatidylcholine (LPC) to phosphatidylcholine (PC), qRT-PCR, western blotting and immunohistochemistry were performed. The correlations of LPCAT1 expression with clinicopathological features and prognosis were assessed. In addition, siRNAs were used to knockdown LPCAT1 expression in ccRCC cell lines, and its effect on cell proliferation, cell cycle, migration and invasion were investigated.

resultsThe phospholipid compositions of ccRCC and normal renal tissues were significantly different. Multiple LPC species were decreased and corresponding PC species were increased in cancer tissues. The mRNA and protein levels of LPCAT1 were up-regulated in ccRCC tissues compared with normal renal tissues, and LPCAT1 expression was significantly correlated with unfavourable pathological features (higher tumour grade, higher TNM stage and larger tumour size) and overall survival. In cell line experiments, LPCAT1 knockdown depleted PCs, inhibited cell proliferation, migration and invasion and induced cell cycle arrest at the G0/G1 phase.

conclusionSelective changes in PC and LPC composition were observed in ccRCC tissues. The overexpression of LPCAT1 promotes the development and progression of ccRCC, likely through the conversion of LPC to PC.

Indexed as

1-Acylglycerophosphocholine O-AcyltransferaseAdultAgedAged, 80 and overCarcinoma, Renal CellCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationFemaleGene Expression ProfilingGene Knockdown TechniquesHumansImmunohistochemistryKidney NeoplasmsMale1-Acylglycerophosphocholine O-AcyltransferaseLpcat1 protein, humanPhospholipidsCancer lipidomicsCarcinomaLPCAT1PhospholipidRenal cell

Identifiers

PMID28494778
PMCPMC5427523
OpenAlexW2613272007

What OpenQuestion holds

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LicenceCC BY
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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.