Evidence map›Paper›PMID 35600335›Full record

ArticleFrontiers in oncology2022

ZKSCAN5 Activates

Jingtong Li, Zhifeng Yan, Jianli Ma, Zhong Chu, Huizi Li, Jingjing Guo, Qingyuan Zhang, Hui Zhao, Ying Li, Tao Wang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. 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
1.4field-weighted citation impact, top 17% 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.

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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

10 authors at 4 institutions in 1 country.

Jingtong LiDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Zhifeng YanDepartment of Obstetrics and Gynecology, Seventh Medical Center of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Jianli MaDepartment of Radiation Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Zhong ChuDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Huizi LiDepartment of Nutrition, People's Liberation Army (PLA) Rocket Force Characteristic Medical Center, Beijing, China.
Jingjing GuoDepartment of Oncology, Fourth Medical Center of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Qingyuan ZhangDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Hui ZhaoDepartment of Oncology, Fourth Medical Center of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Ying LiDepartment of Oncology, Fifth Medical Center of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Tao WangDepartment of Oncology, Fifth Medical Center of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Chinese PLA General Hospital · CNThird Affiliated Hospital of Harbin Medical University · CNChinese People's Liberation Army · CNHarbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The growth of lymphatic vessels (lymphangiogenesis) plays a pivotal role in breast cancer progression and metastasis and the immune response. Vascular endothelial growth factor C (VEGFC) has been demonstrated to accelerate cancer metastasis and modulate the immune system by enhancing lymphangiogenesis. However, it remains largely unclear how transcription factors physically regulate VEGFC expression by interacting with histone-modifying enzymes. Like many histone-modifying enzymes, SETD7 plays a key role in cell proliferation and inhibits tumour cell differentiation. In this study, we identified the role of the transcription factor zinc finger with KRAB and SCAN domains 5 (ZKSCAN5) in interacting with histone methyltransferase SETD7 and mediating VEGFC transcription and tumour lymphangiogenesis. ZKSCAN5 interacts with and recruits SETD7 to the VEGFC promoter. By regulating breast cancer-secreted VEGFC, ZKSCAN5 could induce the tube formation of lymph endothelial cells, which promotes tumour proliferation, migration, and metastasis. Clinically, the expression of ZKSCAN5 was frequently upregulated in patients with breast cancer and positively correlated with the expression of VEGFC and the number of lymphatic microvessels. ZKSCAN5 is a poor prognostic factor for patients with breast cancer. Our results characterise the role of ZKSCAN5 in regulating VEGFC transcription and predict ZKSCAN5 as a breast cancer therapeutic target.

Indexed as

breast cancerlymphangiogenesisproliferation and metastasisSETD7VEGFCZKSCAN5

Identifiers

PMID35600335
PMCPMC9117617
OpenAlexW4229013651

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.