Evidence map›Paper›PMID 31362668›Full record

ArticleCurrent drug metabolism2019

Dysregulation of lncRNA and circRNA Expression in Mouse Testes after Exposure to Triptolide.

Suping Xiong, Yanting Li, Yang Xiang, Na Peng, Chunmiao Shen, Yanqiu Cai, Dandan Song, Peng Zhang, Xiaolong Wang, Xuihui Zeng and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Current drug metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
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  3. Non-hormonal Contraception: Current and Emerging Targets.Advances in experimental medicine and biology · 2025
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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

11 authors at 2 institutions in 1 country.

Suping XiongInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Yanting LiInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Yang XiangInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Na PengInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Chunmiao ShenInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Yanqiu CaiInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Dandan SongInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Peng ZhangInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Xiaolong WangTraditional Chinese Medicine Department, Jilin Women and Children Health Hospital, Changchun, China.
Xuihui ZengInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Xiaoning ZhangInstitute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Nanchang University · CNJilin Maternity and Child Health Care Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTriptolide has been shown to exert various pharmacological effects on systemic autoimmune diseases and cancers. However, its severe toxicity, especially reproductive toxicity, prevents its widespread clinical use for people with fertility needs. Noncoding RNAs including lncRNAs and circRNAs are novel regulatory molecules that mediate a wide variety of physiological activities; they are crucial for spermatogenesis and their dysregulation might cause male infertility. However, whether they are involved in triptolide-induced reproductive toxicity is completely unknown.

methodsAfter exposure of mice to triptolide, the total RNAs were used to investigate lncRNA/circRNA/mRNA expression profiles by strand-specific RNA sequencing at the transcriptome level to help uncover RNA-related mechanisms in triptolide-induced toxicity.

resultsTriptolide significantly decreased testicular weight, damaged testis and sperm morphology, and reduced sperm motility and density. Remarkable deformities in sperm head and tail were also found in triptolide-exposed mice. At the transcriptome level, the triptolide-treated mice exhibited aberrant expression profiles of lncRNAs/circRNAs/mRNAs. Gene Ontology and pathway analyses revealed that the functions of the differentially expressed lncRNA targets, circRNA cognate genes, and mRNAs were closely linked to many processes involved in spermatogenesis. In addition, some lncRNAs/circRNAs were greatly upregulated or inducibly expressed, implying their potential value as candidate markers for triptolide-induced male reproductive toxicity.

conclusionThis study provides a preliminary database of triptolide-induced transcriptome, promotes understanding of the reproductive toxicity of triptolide, and highlights the need for research on increasing the medical efficacy of triptolide and decreasing its toxicity.

Indexed as

RNA, CircularRNA, Long NoncodingAnimalsAntispermatogenic AgentsDiterpenesEpoxy CompoundsMaleMice, Inbred C57BLPhenanthrenesRNA, MessengerSpermatogenesisSpermatozoaSperm MotilityTestisTranscriptomeAntispermatogenic AgentsDiterpenesEpoxy CompoundsPhenanthrenesRNA, CircularRNA, Long NoncodingRNA, MessengertriptolidecircRNAlncRNAmale infertilityRNA sequencingspermatogenesis.Triptolide

Identifiers

PMID31362668
PMCPMC7062010
OpenAlexW2964800100

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.