Evidence map›Paper›PMID 32103167›Full record

ArticleOncogene2020

C1orf35 contributes to tumorigenesis by activating c-MYC transcription in multiple myeloma.

Sai-Qun Luo, De-Hui Xiong, Jiang Li, Guangdi Li, Yali Wang, Jia-Ming Zhang, Xiu-Fen Bu, Wei-Xin Hu, Jingping Hu

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2020. 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
1.1field-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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Prognostic value ofClinical and experimental medicine · 2023
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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

9 authors at 1 institution in 1 country.

Sai-Qun LuoMolecular Biology Research Center, School of Life Science, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
De-Hui XiongMolecular Biology Research Center, School of Life Science, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Jiang LiMolecular Biology Research Center, School of Life Science, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Guangdi LiDepartment of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Yali WangDepartment of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Jia-Ming ZhangMolecular Biology Research Center, School of Life Science, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Xiu-Fen BuMolecular Biology Research Center, School of Life Science, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Wei-Xin HuMolecular Biology Research Center, School of Life Science, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China. weixinhu@mail.csu.edu.cn.
Jingping HuMolecular Biology Research Center, School of Life Science, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China. jingpinghu@csu.edu.cn.ORCID http://orcid.org/0000-0001-5548-1241
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a clinically and biologically heterogenous event that accounts for approximately 10% of all hematological malignancies. Chromosome 1 open reading frame 35 (C1orf35) is a gene cloned and identified in our laboratory from a MM cell line (GenBank: AY137773), but little is known about its function. In the current study, we have confirmed that C1orf35 is a candidate oncogene, and it can promote cell cycle progression from G1 to S. Later, we found that C1orf35 is able to affect the cell proliferation by modulating the expression of c-MYC (v-myc myelocytomatosis viral oncogene homolog), and the oncogenic property of C1orf35 can be rescued by c-MYC inhibition. Herein, we found positive association between C1orf35 and c-MYC in MM patients and in MM cell lines. The correlation analysis of the genes coamplified in MM patients from GEO datasets showed a correlation between C1orf35 and c-MYC, and the expression data of different stages of plasma cell neoplasm acquired from GEO datasets showed that the expression of C1orf35 increase with the progression of the disease. This indicates that C1orf35 may play a role in the disease progression. Moreover, C1orf35 can modulate c-MYC expression and rescue c-MYC transcription inhibited by Act D. Finally, we have shown that C1orf35 activates c-MYC transcription by binding to the i-motif of Nuclease hypersensitivity element III

Indexed as

AdultAgedAnimalsCarcinogenesisCell Line, TumorCell ProliferationFemaleHumansMaleMiceMiddle AgedMultiple MyelomaNeoplasm ProteinsNIH 3T3 CellsPromoter Regions, GeneticProtein BindingC1orf35 protein, humanMYC protein, humanNeoplasm ProteinsProto-Oncogene Proteins c-myc

Identifiers

PMID32103167
OpenAlexW3008619668

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.