Evidence map›Paper›PMID 17554518›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2007

Recombinant full-length human IgG1s targeting hormone-refractory prostate cancer.

Bin Liu, Fraser Conrad, Audrey Roth, Daryl C Drummond, Jeff P Simko, James D Marks

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

6 authors at 2 institutions in 1 country.

Bin LiuDepartment of Anesthesia, University of California at San Francisco, 1001 Potrero Avenue, 3C-38, San Francisco, CA 94110, USA. liub@anesthesia.ucsf.edu
Fraser Conrad
Audrey Roth
Daryl C Drummond
Jeff P Simko
James D Marks
University of California, San Francisco · USHermes Microvision (United States) · US

Funding

UCSF PROSTATE CANCER SPOREP50CA089520 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CARROLL, PETER R · 2000 to 2008
$13.9M
Mapping a clinically significant internalizing tumor epitope space.R01CA118919 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LIU, BIN · 2006 to 2013
$2.5M
Internalizing antibody-targeted nanosized siRNA therapeuticsR21CA135586 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LIU, BIN · 2009 to 2010
$374k
Selection of internalizing human antibodies targeting pancreatic tumor cells in sR21CA137429 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LIU, BIN · 2009 to 2010
$374k
Tumor specific cell surface epitope: molecular evolutionR21DK066429 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI LIU, BIN · 2004 to 2005
$303k
NCI NIH HHS P50 CA89520NCI NIH HHS R01 CA118919NCI NIH HHS R01CA118919NCI NIH HHS R21 CA135586NCI NIH HHS R21 CA137429NIDDK NIH HHS R21 DK066429
6 · The paper itself

Abstract

We have used a naive human single-chain fragment variable (scFv) library as a source of random shape repertoire to directly probe the altered surface chemistry of tumor cells. We reported previously the identification of more than 90 internalizing phage monoclonal antibodies targeting prostate cancer cells, including those that are hormone refractory. In this report, we describe the conversion of a panel of those scFvs into full-length human immunoglobulins (IgGs) and show that tumor specificity is retained. We have further shown that antibodies isolated from a naive phage display library can nevertheless be of high affinity towards target tumor cells. In addition, full-length IgGs retain the functionality of parental scFvs including the ability to rapidly enter target cells through receptor-mediated endocytosis and thereby to mediate efficient and specific intracellular payload delivery to tumor cells. We have used recombinant IgGs to immunoprecipitate target antigens and analyzed their molecular composition by mass spectrometry. We have identified one target antigen as activated leukocyte cell adhesion molecule (ALCAM)/MEMD/CD166 and have further studied tissue specificity of this internalizing ALCAM epitope by immunohistochemistry. Our study shows that cell type-specific internalizing human antibody can be readily identified from a naive phage antibody display library, characterized with regards to sequence, affinity, tissue specificity, and antigen identity, and modified genetically and chemically to generate various forms of targeted therapeutics.

Indexed as

Activated-Leukocyte Cell Adhesion MoleculeAmino Acid SequenceAnimalsAntibodies, NeoplasmCarcinomaCell Line, TumorCHO CellsCricetinaeCricetulusEndocytosisHumansImmunoglobulin GImmunoglobulin Variable RegionImmunohistochemistryImmunoprecipitationImmunotherapyActivated-Leukocyte Cell Adhesion MoleculeAntibodies, NeoplasmImmunoglobulin GImmunoglobulin Variable RegionLiposomesPeptide LibraryProstate-Specific AntigenRecombinant Proteins

Identifiers

PMID17554518
OpenAlexW2159919187

What OpenQuestion holds

Textmetadata
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.