Evidence map›Paper›PMID 33828526›Full record

ArticleFrontiers in endocrinology2021

Seven Novel Genes Related to Cell Proliferation and Migration of VHL-Mutated Pheochromocytoma.

Shuai Gao, Longfei Liu, Zhuolin Li, Yingxian Pang, Jiaqi Shi, Feizhou Zhu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Shuai GaoDepartment of Biochemistry and Molecular Biology, School of Life Sciences, Central South University, Changsha, China.
Longfei LiuDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Zhuolin LiDepartment of Biochemistry and Molecular Biology, School of Life Sciences, Central South University, Changsha, China.
Yingxian PangDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Jiaqi ShiDepartment of Biochemistry and Molecular Biology, School of Life Sciences, Central South University, Changsha, China.
Feizhou ZhuDepartment of Biochemistry and Molecular Biology, School of Life Sciences, Central South University, Changsha, China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pheochromocytoma, as a neuroendocrine tumor with the highest genetic correlation in all types of tumors, has attracted extensive attention. Von Hipper Lindau (VHL) has the highest mutation frequency among the genes associated with pheochromocytoma. However, the effect of VHL on the proteome of pheochromocytoma remains to be explored. In this study, the VHL knockdown (VHL-KD) PC12 cell model was established by RNA interference (shRNA). We compared the proteomics of VHL-KD and VHL-WT PC12 cell lines. The results showed that the expression of 434 proteins (VHL shRNA/WT > 1.3) changed significantly in VHL-KD-PC12 cells. Among the 434 kinds of proteins, 83 were involved in cell proliferation, cell cycle and cell migration, and so on. More importantly, among these proteins, we found seven novel key genes, including Connective Tissue Growth Factor (CTGF), Syndecan Binding Protein (SDCBP), Cysteine Rich Protein 61 (CYR61/CCN1), Collagen Type III Alpha 1 Chain (COL3A1), Collagen Type I Alpha 1 Chain (COL1A1), Collagen Type V Alpha 2 Chain (COL5A2), and Serpin Family E Member 1 (SERPINE1), were overexpressed and simultaneously regulated cell proliferation and migration in VHL-KD PC12 cells. Furthermore, the abnormal accumulation of HIF2α caused by VHL-KD significantly increased the expression of these seven genes during hypoxia. Moreover, cell-counting, scratch, and transwell assays demonstrated that VHL-KD could promote cell proliferation and migration, and changed cell morphology. These findings indicated that inhibition of VHL expression could promote the development of pheochromocytoma by activating the expression of cell proliferation and migration associated genes.

Indexed as

Cell MovementCell ProliferationAdrenal Gland NeoplasmsCollagen Type I, alpha 1 ChainCollagen Type IIICollagen Type VConnective Tissue Growth FactorCysteine-Rich Protein 61HumansMutationPheochromocytomaSynteninsVon Hippel-Lindau Tumor Suppressor ProteinCCN1 protein, humanCCN2 protein, humanCOL1A1 protein, humanCOL3A1 protein, humanCollagen Type I, alpha 1 ChainCollagen Type IIICollagen Type VConnective Tissue Growth FactorCysteine-Rich Protein 61SDCBP protein, humanSynteninsVon Hippel-Lindau Tumor Suppressor Proteincellular communication network factor 1 (CCN1)collagen type III alpha 1 chain (COL3A1)collagen type V alpha 2 chain (COL5A2)connective tissue growth factor (CTGF)pheochromocytomaserpin family E member 1 (SERPINE1)syndecan binding protein (SDCBP)Von Hippel-Lindau (VHL)

Identifiers

PMID33828526
PMCPMC8021008
OpenAlexW3136868961

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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.