Evidence map›Paper›PMID 23913163›Full record

ArticleMolecular cancer research : MCR2013

Inhibition of cell adhesion by a cadherin-11 antibody thwarts bone metastasis.

Yu-Chen Lee, Mehmet Asim Bilen, Guoyu Yu, Song-Chang Lin, Chih-Fen Huang, Angelica Ortiz, Hyojin Cho, Jian H Song, Robert L Satcher, Jian Kuang and 4 more

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  4. Targeting breast and pancreatic cancer metastasis using a dual-cadherin antibody.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

14 authors at 3 institutions in 2 countries.

Yu-Chen Lee *Departments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Mehmet Asim Bilen *Departments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Guoyu Yu *Departments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Song-Chang LinDepartments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Chih-Fen HuangDepartments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Angelica OrtizDepartments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Hyojin ChoDepartments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Jian H SongDepartments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Robert L SatcherDepartments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Jian KuangDepartments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Gary E GallickDepartments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Li-Yuan Yu-LeeDepartment of Medicine, Baylor College of Medicine, Houston, Texas.
Wilber HuangAbnova Corporation, Taiwan.
Sue-Hwa LinDepartments of Translational Molecular Pathology, Genitourinary Medical Oncology, Orthopaedic Oncology, Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Baylor College of Medicine · USNational Taiwan University Hospital · TWThe University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Targeting Tumor Microenvironment-Induced Therapy Resistance in Prostate Cancer Bone MetastasisP50CA140388 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOGOTHETIS, CHRISTOPHER J., THOMPSON, TIMOTHY CHARLES · 2009 to 2022
$23.4M
Endothelial-to-osteoblast transition in prostate cancer bone metastasisR01CA174798 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIN, SUE-HWA · 2013 to 2023
$3.0M
Bone Metastasis Factor-1 in Prostate Cancer/Bone InteractionR01CA111479 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIN, SUE-HWA · 2005 to 2009
$1.3M
NCI NIH HHS CA111479NCI NIH HHS CA16647NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA140388NCI NIH HHS P50-CA140388NCI NIH HHS R01 CA111479NCI NIH HHS R01 CA174798
6 · The paper itself

Abstract

unlabelledCadherin-11 (CDH11) is a member of the cadherin superfamily mainly expressed in osteoblasts but not in epithelial cells. However, prostate cancer cells with a propensity for bone metastasis express high levels of cadherin-11 and reduced levels of E-cadherin. Downregulation of cadherin-11 inhibits interaction of prostate cancer cells with osteoblasts in vitro and homing of prostate cancer cells to bone in an animal model of metastasis. These findings indicate that targeting cadherin-11 may prevent prostate cancer bone metastasis. To explore this possibility, a panel of 21 monoclonal antibodies (mAb) was generated against the extracellular (EC) domain of cadherin-11. Two antibodies, mAbs 2C7 and 1A5, inhibited cadherin-11-mediated cell-cell aggregation in vitro using L-cells transfected with cadherin-11. Both antibodies demonstrated specificity to cadherin-11, and neither antibody recognized E-cadherin or N-cadherin on C4-2B or PC3 cells, respectively. Furthermore, mAb 2C7 inhibited cadherin-11-mediated aggregation between the highly metastatic PC3-mm2 cells and MC3T3-E1 osteoblasts. Mechanistically, a series of deletion mutants revealed a unique motif, aa 343-348, in the cadherin-11 EC3 domain that is recognized by mAb 2C7 and that this motif coordinated cell-cell adhesion. Importantly, administration of mAb 2C7 in a prophylactic setting effectively prevented metastasis of PC3-mm2 cells to bone in an in vivo mouse model. These results show that targeting the extracellular domain of cadherin-11 can limit cellular adhesion and metastatic dissemination of prostate cancer cells. IMPLICATIONS: Monotherapy using a cadherin-11 antibody is a suitable option for the prevention of bone metastases.

Indexed as

Neoplasm MetastasisAnimalsAntibodies, MonoclonalBinding Sites, AntibodyBone NeoplasmsCadherinsCell AdhesionCell MovementEpitope MappingHumansMaleMiceMice, SCIDMutationProstatic NeoplasmsAntibodies, MonoclonalCadherinsosteoblast cadherin

Identifiers

PMID23913163
PMCPMC3834228
OpenAlexW2160853823

What OpenQuestion holds

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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.