Evidence map›Paper›PMID 30622325›Full record

ArticleCancer gene therapy2020

Prognosis value of RBBP8 expression in plasma cell myeloma.

Weilong Zhang, Ying Song, Xue He, Xiaoni Liu, Ye Zhang, Zuozhen Yang, Ping Yang, Jing Wang, Kai Hu, Weiyou Liu and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer gene therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  7. Review
  8. The lncRNAsMolecular therapy. Nucleic acids · 2021
    Article
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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

13 authors at 5 institutions in 2 countries.

Weilong Zhang *Department of Hematology, Lymphoma Research Center, Peking University Third Hospital, Beijing, 100191, China.
Ying Song *Gannan Medical University, Ganzhou, 341000, China.
Xue He *Department of Pathology, Beijing Tiantan Hospital Affiliated with Capital Medical University, No. 6 Tiantan Xili, Beijing, 100050, China.ORCID http://orcid.org/0000-0003-4448-5399
Xiaoni LiuDepartment of Respiratory Medicine, The First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, China.
Ye ZhangMelbourne School of Population and Global Health, The University of Melbourne, Victoria, 3010, Australia.
Zuozhen YangDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, Beijing, 100191, China.
Ping YangDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, Beijing, 100191, China.
Jing WangDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, Beijing, 100191, China.
Kai HuDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, Beijing, 100191, China.
Weiyou LiuDepartment of Respiratory Medicine, The First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, China.
Xiuru ZhangDepartment of Pathology, Beijing Tiantan Hospital Affiliated with Capital Medical University, No. 6 Tiantan Xili, Beijing, 100050, China. zhangxiuru999@163.com.
Xiaoliang YuanDepartment of Respiratory Medicine, The First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, China. yxlyyxs@126.com.
Hongmei JingDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, Beijing, 100191, China. drjinghm@163.com.
Peking University · CNFirst Affiliated Hospital of Gannan Medical University · CNCapital Medical University · CNGannan Medical University · CNThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasma cell myeloma (PCM) secretes monoclonal immunoglobulin (Ig) by clonal plasma cells of abnormal proliferation in the bone marrow. As PCM is incurable, it is necessary to find new biomarkers to predict the prognosis and recurrence of PCM. The relationship between cancer and RBBP8 has not been fully studied. The role of RBBP8 in tumorigenesis remains inconsistent. We described the expression of RBBP8 in the gene expression profile of 1930 PCM samples (1878 PCM patients) from seven independent data sets. We analyzed the relationship between RBBP8 and survival prognosis, recurrence, and treatment response in patients with PCM, and the biological significance of RBBP8 in PCM. The gene expression level of RBBP8 was significantly related to the International staging system (ISS) grade of PCM (P = 0.0012). RBBP8 expression in different molecular subtypes was different (P < 2.2e-16). High RBBP8 expression is associated with poor survival in PCM (P < 0.0001). High expression of RBBP8 indicates that PCM patients are more likely to relapse (P = 0.0078). The biological significance of RBBP8 in PCM is related to the cell cycle (P < 0.05). High RBBP8 expression predicts poorer survival and more likely relapse in PCM. RBBP8 plays an important role in the cell cycle of PCM. RBBP8 can be considered an independent prognostic factor for PCM. RBBP8 can be used as a potential biomarker for assessing the prognosis of PCM patients.

Indexed as

Gene Expression Regulation, NeoplasticAgedBiomarkers, TumorBone MarrowCarcinogenesisCell CycleDatasets as TopicDisease-Free SurvivalEndodeoxyribonucleasesFemaleGene Expression ProfilingHumansKaplan-Meier EstimateMaleMiddle AgedMultiple MyelomaBiomarkers, TumorEndodeoxyribonucleasesRBBP8 protein, human

Identifiers

PMID30622325
PMCPMC7027984
OpenAlexW2908556673

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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.