Evidence map›Paper›PMID 26472025›Full record

ArticleOncotarget2015

Aberrant high expression of immunoglobulin G in epithelial stem/progenitor-like cells contributes to tumor initiation and metastasis.

Qinyuan Liao, Wei Liu, Yang Liu, Fulin Wang, Chong Wang, Jingxuan Zhang, Ming Chu, Dongyang Jiang, Lin Xiao, Wenwei Shao and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

39 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Immunoglobulin G in aging and cancer.Frontiers in immunology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Non B Cell-Derived Immunoglobulins in Lung Epithelial Cells and Lung Cancer.Advances in experimental medicine and biology · 2024
    Review
  10. Review
  11. Article
  12. Non B Cell-Derived Immunoglobulin, A Brighter Horizon for the Future.Advances in experimental medicine and biology · 2024
    Review
  13. Review
  14. Review
  15. The Expression of Non B Cell-Derived Immunoglobulins.Advances in experimental medicine and biology · 2024
    Review
  16. Comparison of Non B-Ig and B-Ig.Advances in experimental medicine and biology · 2024
    Review
  17. Expression and Function of Mammary Epithelial Cell-Derived Immunoglobulins.Advances in experimental medicine and biology · 2024
    Review
  18. Non B Cell-Derived Immunoglobulins in Intestinal Tract.Advances in experimental medicine and biology · 2024
    Review
  19. Article
  20. Article
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

19 authors at 6 institutions in 3 countries.

Qinyuan LiaoDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Wei LiuDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Yang LiuDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Fulin WangDepartment of Pathology, Chinese PLA General Hospital, Beijing, 100853, China.
Chong WangDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Jingxuan ZhangKey Laboratory of Medical Immunology, Ministry of Health, Beijing, 100191, China.
Ming ChuDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Dongyang JiangDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Lin XiaoDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Wenwei ShaoDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Zhengzuo ShengDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Xia TaoDepartment of Gynecology, Peking University First Hospital, Beijing, 100034, China.
Lei HuoDivision of Pathology and Laboratory Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, 77030, USA.
C Cameron YinDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, 77030, USA.
Youhui ZhangDepartment of Immunology, Cancer Institute & Hospital, Chinese Academy of Medical Science, Beijing, 100021, China.
Gregory LeeAndrology Laboratory, University of British Columbia Centre for Reproductive Health, Vancouver, BC V5Z 4H4, Canada.
Jing HuangDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Zihai LiDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC 29425, USA.
Xiaoyan QiuDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Peking University · CNThe University of Texas MD Anderson Cancer Center · USChinese Academy of Medical Sciences & Peking Union Medical College · CNChinese PLA General Hospital · CNMedical University of South Carolina · USUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High expression of immunoglobulin G (IgG) in many non-B cell malignancies and its non-conventional roles in promoting proliferation and survival of cancer cells have been demonstrated. However, the precise function of non-B IgG remains incompletely understood. Here we define the antigen specificity of RP215, a monoclonal antibody that specifically recognizes the IgG in cancer cells. Using RP215, our study shows that IgG is overexpressed in cancer cells of epithelial lineage, especially cells with cancer stem/progenitor cell-like features. The RP215-recognized IgG is primarily localized on the cell surface, particularly lamellipodia-like structures. Cells with high IgG display higher migration, increased invasiveness and metastasis, and enhanced self-renewal and tumorgenecity ability in vitro and in vivo. Importantly, depletion of IgG in breast cancer leads to reduced adhesion, invasion and self-renewal and increased apoptosis of cancer cells. We conclude that high expression of IgG is a novel biomarker of tumor progression, metastasis and cancer stem cell maintenance and demonstrate the potential therapeutic benefits of RP215-recognized IgG targeted strategy.

Indexed as

AnimalsAntibodies, MonoclonalBlotting, WesternBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationEpithelial CellsFemaleGene ExpressionHumansImmunoglobulin GImmunohistochemistryMatrix Metalloproteinase 2Matrix Metalloproteinase 9MCF-7 CellsAntibodies, MonoclonalImmunoglobulin GMatrix Metalloproteinase 2Matrix Metalloproteinase 9epithelial stem/progenitor-like cellsIgGRP215tumor metastasis

Identifiers

PMID26472025
PMCPMC4741881
OpenAlexW1897668916

What OpenQuestion holds

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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.