Evidence map›Paper›PMID 26334999›Full record

ArticleBMC cancer2015

Patient-derived heavy chain antibody targets cell surface HSP90 on breast tumors.

Charan V Devarakonda, Daniel Kita, Kathryn N Phoenix, Kevin P Claffey

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Heat Shock Proteins in Lymphoma Immunotherapy.Frontiers in immunology · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. 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

4 authors at 1 institution in 1 country.

Charan V DevarakondaDepartment of Cell Biology, Center for Vascular Biology, University of Connecticut Health Center, 263 Farmington Avenue, Lab E5029, Farmington, CT-06030-3501, USA. charankumardvs@gmail.com.
Daniel KitaDepartment of Cell Biology, Center for Vascular Biology, University of Connecticut Health Center, 263 Farmington Avenue, Lab E5029, Farmington, CT-06030-3501, USA. kita@uchc.edu.
Kathryn N PhoenixDepartment of Cell Biology, Center for Vascular Biology, University of Connecticut Health Center, 263 Farmington Avenue, Lab E5029, Farmington, CT-06030-3501, USA. knphoenix16@gmail.com.
Kevin P ClaffeyDepartment of Cell Biology, Center for Vascular Biology, University of Connecticut Health Center, 263 Farmington Avenue, Lab E5029, Farmington, CT-06030-3501, USA. claffey@uchc.edu.
UConn Health · US

Funding

Discovery Platform for Cancer AntigensR33CA143531 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI CLAFFEY, KEVIN P. · 2010 to 2012
$1.2M
NCI NIH HHS R33 CA143531NCI NIH HHS R33 CA1453531-01
6 · The paper itself

Abstract

backgroundMonoclonal antibodies have been used to effectively treat various tumors. We previously established a unique strategy to identify tumor specific antibodies by capturing B-cell response against breast tumor antigens from patient-derived sentinel lymph nodes. Initial application of this approach led to identification of a tumor specific single domain antibody. In this paper we optimized our previous strategy by generating heavy chain antibodies (HCAbs) to overcome the deficiencies of single domain antibodies. Here we identified and characterized a heavy chain antibody (HCAb2) that targets cell surface HSP90 antigen on breast tumor cells but not normal cells.

methodsEight HCAbs derived from 4 breast cancer patients were generated using an in vitro expression system. HCAbs were screened against normal breast cells (MCF10A, HMEC) and tumor cell lines (MCF7, MDA-MB-231) to identify cell surface targeting and tumor specific antibodies using flow cytometry and immunofluorescence. Results observed with cell lines were validated by screening a cohort of primary human breast normal and tumor tissues using immunofluorescence. Respective antigens for two HCAbs (HCAb1 and HCAb2) were identified using immunoprecipitation followed by mass spectrometry. Finally, we generated MDA-MB-231 xenograft tumors in NOD scid gamma mice and performed in vivo tumor targeting analysis of HCAb1 and HCAb2.

resultsFlow cytometry screen revealed that HCAb2 selectively bound to the surface of MDA-MB-231 cells in comparison to MCF10A and MCF7 cells. HCAb2 showed punctate membrane staining on MDA-MB-231 cells and preferential binding to human breast tumor tissues in comparison to normal breast tissues. In primary breast tumor tissues, HCAb2 showed positive binding to both E-cadherin positive and negative tumor cells. We identified and validated the target antigen of HCAb2 as Heat shock protein 90 (HSP90). HCAb2 also selectively targeted MDA-MB-231 xenograft tumor cells in vivo with little targeting to mouse normal tissues. Finally, HCAb2 specifically targeted calnexin negative xenograft tumor cells.

conclusionsFrom our screening methodology, we identified HCAb2 as a breast tumor specific heavy chain antibody targeting cell surface HSP90. HCAb2 also targeted MDA-MB-231 tumor cells in vivo suggesting that HCAb2 could be an ideal tumor targeting antibody.

Indexed as

AnimalsAntibodies, NeoplasmBreast NeoplasmsCell Line, TumorFemaleFlow CytometryHeterograftsHSP90 Heat-Shock ProteinsHumansImmunoglobulin Heavy ChainsImmunoprecipitationMass SpectrometryMiceMice, SCIDRNA, Small InterferingAntibodies, NeoplasmHSP90 Heat-Shock ProteinsImmunoglobulin Heavy ChainsRNA, Small Interfering

Identifiers

PMID26334999
PMCPMC4559304
OpenAlexW1939999801

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.