Evidence map›Paper›PMID 27588468›Full record

ArticleOncotarget2016

Oxysterol-binding protein-related protein 4L promotes cell proliferation by sustaining intracellular Ca2+ homeostasis in cervical carcinoma cell lines.

Ji-Wei Li, Yan-Lin Xiao, Chao-Feng Lai, Ning Lou, Hong-Ling Ma, Bi-Ying Zhu, Wen-Bin Zhong, Dao-Guang Yan

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Roles of calcium in ameloblasts during tooth development: A scoping review.Journal of Taibah University Medical Sciences · 2025
    Review
  2. Oxysterols as Biomarkers of Aging and Disease.Advances in experimental medicine and biology · 2024
    Article
  3. How does NFAT3 regulate the occurrence of cardiac hypertrophy?International journal of cardiology. Heart & vasculature · 2023
    Review
  4. Observational
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. The Role of Oxysterols in Human Cancer.Trends in endocrinology and metabolism: TEM · 2017
    Review
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

8 authors at 2 institutions in 1 country.

Ji-Wei LiDepartment of Biotechnology, Jinan University, Guangzhou, 510632, China.
Yan-Lin XiaoDepartment of Biotechnology, Jinan University, Guangzhou, 510632, China.
Chao-Feng LaiDepartment of Biotechnology, Jinan University, Guangzhou, 510632, China.
Ning LouState Key Laboratory of Oncology in Southern China, Collaborative Innovation Center of Cancer Medicine, Guangzhou, 510060, China.
Hong-Ling MaDepartment of Biotechnology, Jinan University, Guangzhou, 510632, China.
Bi-Ying ZhuDepartment of Biotechnology, Jinan University, Guangzhou, 510632, China.
Wen-Bin ZhongDepartment of Biotechnology, Jinan University, Guangzhou, 510632, China.
Dao-Guang YanDepartment of Biotechnology, Jinan University, Guangzhou, 510632, China.
Jinan University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxsterol binding protein-related protein 4 (ORP4) is essential for cell proliferation, but the underlying mechanism is unclear. ORP4 is expressed as three variants, ORP4L, ORP4M and ORP4S. Here, we reported that silencing of ORP4L with specific small interfering RNA (siRNA) inhibited the proliferation of human cervical cancer cell lines C33A, HeLa and CaSki, the reverse effect being observed in ORP4L overexpressing cells. For molecular insight, we found that ORP4L maintained intracellular Ca2+ homeostasis. Through this mechanism, ORP4L activated nuclear factor of activated T cells (NFAT) activity and thus promoted expression of a gene cluster which supported cell proliferation. Of note, ORP4L sustained inositol-1,4,5-trisphosphate receptor 1 (IP3R1) expression at both mRNA and protein levels via Ca2+-dependent NFAT3 activation, which offered a mechanic explanation for the role of ORP4L intracellular Ca2+ homeostasis. Furthermore, ORP4L knockdown markedly inhibited tumor growth in a C33A cell xenograft mouse model. To conclude, our results reveal that ORP4L promotes cell proliferation through maintaining intracellular Ca2+ homeostasis.

Indexed as

Cell ProliferationAnimalsApoptosisBiomarkers, TumorCalciumCytoplasmFemaleHomeostasisHumansInositol 1,4,5-Trisphosphate ReceptorsMaleMiceMice, Inbred BALB CMice, NudeNFATC Transcription FactorsOxysterol Binding ProteinsBiomarkers, TumorCalciumInositol 1,4,5-Trisphosphate ReceptorsITPR1 protein, humanNFATC Transcription FactorsOxysterol Binding ProteinsOxysterolsProtein IsoformsReceptors, SteroidCa2+ homeostasisIP3R1NFATORP4Lproliferation

Identifiers

PMID27588468
PMCPMC5323197
OpenAlexW2518078251

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.