Evidence map›Paper›PMID 28858294›Full record

ArticleActa pharmacologica Sinica2018

The ceramide pathway is involved in the survival, apoptosis and exosome functions of human multiple myeloma cells in vitro.

Qian Cheng, Xin Li, Yue Wang, Min Dong, Feng-Huang Zhan, Jing Liu

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

62 citing papers in PubMed, 103 citations in OpenAlex.

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  19. Emerging role of exosomes in hematological malignancies.Clinical and experimental medicine · 2023
    Review
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2 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 2 countries.

Qian ChengDepartment of Hematology, the Third Xiangya Hospital of Central South University, Changsha 412000, China.
Xin LiDepartment of Hematology, the Third Xiangya Hospital of Central South University, Changsha 412000, China.
Yue WangDepartment of Hematology, the Affiliated Hospital of Guilin Medical College, Guilin 541000, China.
Min DongDepartment of Hematology, the Affiliated Hospital of Guilin Medical College, Guilin 541000, China.
Feng-Huang ZhanDepartment of Medicine, Division of Hematology, University of Iowa, Iowa City, IA USA.
Jing LiuDepartment of Hematology, the Third Xiangya Hospital of Central South University, Changsha 412000, China.
Affiliated Hospital of Guilin Medical College · CNThird Xiangya Hospital · CNCentral South University · CNUniversity of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
6 · The paper itself

Abstract

Multiple myeloma (MM) is characterized by the clonal proliferation of malignant plasma cells and refractoriness to traditional therapies. It has been shown that exosomes are involved in modulating the progression and the metastasis of cancers through microRNAs (miRs). Ceramide is a type of sphingolipid; the ceramide pathway of exosomal secretion has been shown to affect the apoptosis of cancer cells. But the role of this pathway in MM cell function, exosome function and miR regulation remains unknown. In this study, we showed that C6 ceramide (an exogenous ceramide supplement, 1.25-40 μmol/L) dose-dependently inhibited the proliferation and promoted the apoptosis in human MM OPM2 cell line, which were associated with elevated caspase 3/9 and PARP cleavage. We also found that C6 ceramide (5-20 μmol/L) dose-dependently stimulated exosome secretion and increased exosomal levels of tumor-suppressive miRs (miR 202, miR 16, miR 29b and miR 15a). Of note, exosomes from C6 ceramide-treated OPM2 cells could influence the proliferation and apoptosis of the recipient OPM2 cells, which correlated with increased tumor-suppressive exosomal miRs. In contrast, GW4869 (a ceramide inhibitor, 5-20 μmol/L) exerted the opposite effects on the regulation of MM function, exosome secretion and miR levels in MM exosomes. However, exosomes from GW4869-treated OPM2 cells had no effect on these miRs and the survival of targeted OPM2 cells. Taken together, our findings reveal that the ceramide pathway modulates MM survival, probably directly via the caspase pathway and indirectly via exosomal miR mechanisms.

Indexed as

Aniline CompoundsApoptosisBenzylidene CompoundsCaspasesCell Line, TumorCell ProliferationCell SurvivalCeramidesExosomesHumansMicroRNAsMultiple MyelomaPoly(ADP-ribose) PolymerasesSignal TransductionAniline CompoundsBenzylidene CompoundsCaspasesCeramidesGW 4869MicroRNAsN-caproylsphingosinePoly(ADP-ribose) Polymerases

Identifiers

PMID28858294
PMCPMC5888679
OpenAlexW2751240956

What OpenQuestion holds

Textmetadata
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.