Evidence map›Paper›PMID 40471366›Full record

ArticleCellular and molecular life sciences : CMLS2025

SNORD88B promotes proliferation and invasion of trophoblast by regulating G3BP1 m6 A modification and alternative splicing.

Bingfeng Lu, Qianhui Li, Haiying Wang, Jiachen Cheng, Yuran Zhang, Xi Chen, Baixue Li, Yang Zhao

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

8 authors.

Bingfeng Lu *Department of Obstetrics and Gynecology, Department of Gynecologic Oncology Research Office, Guangzhou Key Laboratory of Targeted Therapy for Gynecologic Oncology, Guangzhou, China.
Qianhui Li *Department of Obstetrics and Gynecology, Department of Gynecologic Oncology Research Office, Guangzhou Key Laboratory of Targeted Therapy for Gynecologic Oncology, Guangzhou, China.
Haiying WangDepartment of Obstetrics and Gynecology, Department of Gynecologic Oncology Research Office, Guangzhou Key Laboratory of Targeted Therapy for Gynecologic Oncology, Guangzhou, China.
Jiachen ChengDepartment of Obstetrics and Gynecology, Department of Gynecologic Oncology Research Office, Guangzhou Key Laboratory of Targeted Therapy for Gynecologic Oncology, Guangzhou, China.
Yuran ZhangDepartment of Obstetrics and Gynecology, Department of Gynecologic Oncology Research Office, Guangzhou Key Laboratory of Targeted Therapy for Gynecologic Oncology, Guangzhou, China.
Xi ChenCancer Hospital of Dalian, Cancer Hospital of China Medical University, University of Technology, Liaoning Cancer Hospital & Institute, Shenyang, China.
Baixue LiDepartment of Obstetrics and Gynecology, Department of Gynecologic Oncology Research Office, Guangzhou Key Laboratory of Targeted Therapy for Gynecologic Oncology, Guangzhou, China.
Yang ZhaoDepartment of Obstetrics and Gynecology, Department of Gynecologic Oncology Research Office, Guangzhou Key Laboratory of Targeted Therapy for Gynecologic Oncology, Guangzhou, China. yida.zhaoyang@163.com.ORCID http://orcid.org/0000-0003-3226-8127

Funding

National Natural Science Foundation of China 82403018Project for Key Medicine Discipline Construction of Guangzhou Municipality 2021-2023-17Science and Technology Projects in Guangzhou 2024A03J0897
6 · The paper itself

Abstract

backgroundSmall nucleolar RNA (snoRNA) has recently been shown to play a key role in different diseases, but how snoRNA works to promote the biological behavior of trophoblast remains unclear.

methodsThe expression of snoRNA in the placental villi of females were detected by RNA-seq and qPCR. RNA immunoprecipitation (RIP), RNA methylation co-immunoprecipitation (Me-RIP), and cell experiments were used to explore the molecular mechanism of SNORD88B in regulating the function of villous trophoblasts.

resultsSNORD88B was down-regulated in the placental villi of patients with spontaneous abortion, while the overexpression of SNORD88B could promote the proliferation, invasion, and migration of villous trophoblast cells. Mechanistically, SNORD88B directly binds to m6A methyltransferase METTL14 to regulate the m6A modification of G3BP1 mRNA and enhances its mRNA stability by recruiting the reader IGF2BP2. Besides, SNORD88B also regulates the alternative splicing of pre-G3BP1 by recruiting splicing factors SRSF1 and U2AF1, which ameliorates the expression of its effective transcripts to further promote the expression of G3BP1 protein.

conclusionsWe investigated the functional roles and the underlying regulatory mechanisms of SNORD88B in the enhancement of villous trophoblasts' development and that under-expressed SNORD88B could contribute to the maldevelopment of placental villi, which may be related to spontaneous abortion.

Indexed as

AdenosineAlternative SplicingRNA HelicasesRNA Recognition Motif ProteinsTrophoblastsAbortion, SpontaneousCell MovementCell ProliferationChorionic VilliDNA HelicasesFemaleHumansMethyltransferasesPoly-ADP-Ribose Binding ProteinsPregnancyRNA-Binding ProteinsAdenosineDNA HelicasesG3BP1 protein, humanIGF2BP2 protein, humanMethyltransferasesMETTL14 protein, humanN-methyladenosinePoly-ADP-Ribose Binding ProteinsRNA-Binding ProteinsRNA HelicasesRNA, MessengerRNA Recognition Motif ProteinsSerine-Arginine Splicing FactorsSRSF1 protein, humanAlternative splicingEarly pregnancy lossG3BP1M6 A modificationSNORD88B

Identifiers

PMID40471366
PMCPMC12141712

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.