Evidence map›Paper›PMID 26429876›Full record

ArticleOncotarget2015

IGK with conserved IGΚV/IGΚJ repertoire is expressed in acute myeloid leukemia and promotes leukemic cell migration.

Chong Wang, Miaoran Xia, Xiaoping Sun, Zhiqiao He, Fanlei Hu, Lei Chen, Carlos E Bueso-Ramos, Xiaoyan Qiu, C Cameron Yin

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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.6field-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

27 citing papers in PubMed, 30 citations in OpenAlex.

  1. Gut Microbiota Dysbiosis MediatesImmunity, inflammation and disease · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Genetic Characteristics of Non B Cell-Derived Immunoglobulin Genes.Advances in experimental medicine and biology · 2024
    Article
  8. Review
  9. Comparison of Non B-Ig and B-Ig.Advances in experimental medicine and biology · 2024
    Review
  10. The Expression of Non B Cell-Derived Immunoglobulins.Advances in experimental medicine and biology · 2024
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. 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

9 authors at 3 institutions in 2 countries.

Chong WangDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, China.
Miaoran XiaDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, China.
Xiaoping SunDepartment of Laboratory Medicine, UT MD Anderson Cancer Center, Houston, TX, USA.
Zhiqiao HeDepartment of Hematopathology, UT MD Anderson Cancer Center, Houston, TX, USA.
Fanlei HuDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, China.
Lei ChenDepartment of Pathology, University of Texas-Houston Medical School, Houston, TX, USA.
Carlos E Bueso-RamosDepartment of Hematopathology, UT MD Anderson Cancer Center, Houston, TX, USA.
Xiaoyan QiuDepartment of Immunology, School of Basic Medical Sciences, Peking University, Beijing, China.
C Cameron YinDepartment of Hematopathology, UT MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · USPeking University · CNThe University of Texas Health Science Center at Houston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously reported that immunoglobulin heavy chain genes were expressed in myeloblasts and mature myeloid cells. In this study, we further demonstrated that rearranged Ig κ light chain was also frequently expressed in acute myeloid leukemia cell lines (6/6), primary myeloblasts from patients with acute myeloid leukemia (17/18), and mature monocytes (11/12) and neutrophils (3/12) from patients with non-hematopoietic neoplasms, but not or only rarely expressed in mature neutrophils (0/8) or monocytes (1/8) from healthy individuals. Interestingly, myeloblasts and mature monocytes/neutrophils shared several restricted IGKV and IGKJ gene usages but with different expression frequency. Surprisingly, almost all of the acute myeloid leukemia-derived IGKV showed somatic hypermutation; in contrast, mature myeloid cells-derived IGKV rarely had somatic hypermutation. More importantly, although IGK expression appeared not to affect cell proliferation, reduced IGK expression led to a decrease in cell migration in acute myeloid leukemia cell lines HL-60 and NB4, whereas increased IGK expression promoted their motility. In summary, IGK is expressed in myeloblasts and mature myeloid cells from patients with non-hematopoietic neoplasms, and is involved in cell migration. These results suggest that myeloid cells-derived IgK may have a role in leukemogenesis and may serve as a novel tumor marker for monitoring minimal residual disease and developing target therapy.

Indexed as

Amino Acid SequenceCell Line, TumorCell MovementCell ProliferationGene RearrangementHL-60 CellsHumansImmunoglobulinsImmunoglobulin Variable RegionLeukemia, Myeloid, AcuteMolecular Sequence DataTransfectionIgKImmunoglobulinsImmunoglobulin Variable Regionacute myeloid leukemiaIgKleukemic cell migrationrestricted IGKV/IGKJ rearrangementsomatic hypermutation

Identifiers

PMID26429876
PMCPMC4770757
OpenAlexW2181165416

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.