Evidence map›Paper›PMID 33450808›Full record

ArticleCancers2021

Mechanical Loading-Driven Tumor Suppression Is Mediated by Lrp5-Dependent and Independent Mechanisms.

Yan Feng, Shengzhi Liu, Rongrong Zha, Xun Sun, Kexin Li, Alexander Robling, Baiyan Li, Hiroki Yokota

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 14 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

8 authors at 4 institutions in 2 countries.

Yan FengDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Harbin 150081, China.
Shengzhi LiuDepartment of Biomedical Engineering, Indiana University Purdue University Indianapolis, Indianapolis, IN 46202, USA.
Rongrong ZhaDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Harbin 150081, China.
Xun SunDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Harbin 150081, China.
Kexin LiDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Harbin 150081, China.
Alexander RoblingDepartment of Anatomy Cell Biology and Physiology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Baiyan LiDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Harbin 150081, China.
Hiroki YokotaDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Harbin 150081, China.
University of Indianapolis · USHarbin Medical University · CNIndiana University Health · USIndiana University School of Medicine

Funding

MECHANICAL LOADING AND BONER01AR052144 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI YOKOTA, HIROKI · 2006 to 2018
$4.2M
Effect of skeletal compression on tumor growth and migrationR03CA238555 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI YOKOTA, HIROKI · 2019 to 2020
$158k
National Cancer Institute, Cairo University R01AR053237NCI NIH HHS R03 CA238555NIAMS NIH HHS R01 AR052144
6 · The paper itself

Abstract

Bone is mechanosensitive and lipoprotein receptor-related protein 5 (Lrp5)-mediated Wnt signaling promotes loading-driven bone formation. While mechanical loading can suppress tumor growth, the question is whether Lrp5 mediates loading-driven tumor suppression. Herein, we examined the effect of Lrp5 using osteocyte-specific Lrp5 conditional knockout mice. All mice presented noticeable loading-driven tumor suppression in the loaded tibia and non-loaded mammary pad. The degree of suppression was more significant in wild-type than knockout mice. In all male and female mice, knee loading reduced cholesterol and elevated dopamine. It reduced tumor-promoting nexin, which was elevated by cholesterol and reduced by dopamine. By contrast, it elevated p53, TNF-related apoptosis-inducing ligand (TRAIL), and chemerin, and they were regulated reversely by dopamine and cholesterol. Notably, Lrp5 overexpression in osteocytes enhanced tumor suppression, and osteoclast development was inhibited by chemerin. Collectively, this study identified Lrp5-dependent and independent mechanisms for tumor suppression. Lrp5 in osteocytes contributed to the loaded bone, while the Lrp5-independent regulation of dopamine- and cholesterol-induced systemic suppression.

Indexed as

breast cancerchemerinLrp5mechanical stimulationnexinosteocyteprostate cancer

Identifiers

PMID33450808
PMCPMC7828232
OpenAlexW3120853873

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.