Evidence map›Paper›PMID 33553338›Full record

ArticleAnnals of translational medicine2021

Roles of NANOGP8 in cancer metastasis and cancer stem cell invasion during development of castration-resistant prostate cancer.

Yi Sui, Wei Zhang, Rujian Zhu, Lili Gao, Ting Cao, Chuhong Chen, Min Gong, Hongbo Zhu, Tao Tang, Bo Yu and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 59% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Review
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 5 institutions in 1 country.

Yi SuiDepartment of Nutrition, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Wei ZhangDepartment of Pharmacology, School of Basic Medicine, Hebei University of Chinese Medicine, Shijiazhuang, China.
Rujian ZhuDepartment of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Lili GaoCenter for Medical Research and Innovation, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Ting CaoCenter for Medical Research and Innovation, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Chuhong ChenDepartment of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Min GongDepartment of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Hongbo ZhuDepartment of Pathology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Tao TangDepartment of Obstetrics and Gynaecology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China.
Bo YuDepartment of General Surgery, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Tao YangCenter for Medical Research and Innovation, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Pudong Medical Center · CNFudan University · CNHebei University of Chinese Medicine · CNPrince of Wales Hospital · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer (PCa) is one of the most common types of cancer and the emerging resistance to androgen deprivation therapy in PCa aggravates disease progression. In this study, we examined the potential pro-tumorigenic functions of NANOGP8 in prostate cancer development.

methodsQuantitative RT-PCR confirmed higher NANOGP8 expression in androgen independent tumors, as well as a recurrent prostate tumor in patient samples. We then established a novel two-way inducible NANOGP8-short hairpin RNA experimental system, in which the NANOGP8 expression was transiently induced by adding doxycycline in the diet of NOD/SCID mice.

resultsThe knockdown of NANOGP8 inhibited implanted tumor growth and the progression of castration-resistant PCa. NANOGP8-deficient PCa cells lost their cancer stem cell and gene expression programs. To further investigate the functions of NANOGP8 in PCa stem cells, real-time cell tracking was used to monitor the cell division modes and differentiation patterns of NANOGP8

conclusionsBased on these findings, we propose that NANOGP8 could serve as an effective therapeutic target for the treatment of PCa.

Indexed as

androgen independent tumorscancer stem cellNANOGP8prostate cancer (PCa)

Identifiers

PMID33553338
PMCPMC7859782
OpenAlexW3123356093

What OpenQuestion holds

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Registered trials

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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.