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Therapeutic targeting of membrane-associated GRP78 in leukemia and lymphoma: Preclinical efficacy in vitro and formal toxicity study of BMTP-78 in rodents and primates

  • D. I. Staquicini
    ,
  • S. D'Angelo
    ,
  • F. Ferrara
    ,
  • K. Karjalainen
    ,
  • G. Sharma
    ,
  • T. L. Smith
*Corresponding author for this work
  • University of New Mexico
    ,
  • Specifica Inc.
    ,
  • University of Texas MD Anderson Cancer Center
    ,
  • American University of Beirut
    ,
  • Sojo University
    ,
  • National Institutes of Health, Bethesda
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Translation of drug candidates into clinical settings requires demonstration of preclinical efficacy and formal toxicology analysis for filling an Investigational New Drug (IND) application with the US Food and Drug Administration (FDA). Here, we investigate the membrane-associated glucose response protein 78 (GRP78) as a therapeutic target in leukemia and lymphoma. We evaluated the efficacy of the GRP78-targeted proapoptotic drug bone metastasis targeting peptidomimetic 78 (BMTP-78), a member of the D (KLAKLAK)2-containing class of agents. BMTP-78 was validated in cells from patients with acute myeloid leukemia and in a panel of human leukemia and lymphoma cell lines, where it induced dose-dependent cytotoxicity in all samples tested. Based on the in vitro efficacy of BMTP-78, we performed formal good laboratory practice toxicology studies in both rodents (mice and rats) and nonhuman primates (cynomolgus and rhesus monkeys). These analyses represent required steps towards an IND application of BMTP-78 for theranostic first-in-human clinical trials.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 436-443 (8 pages)

Journal (Volume, Issue Number)

Pharmacogenomics Journal (Volume 18, Issue 3)

Publication milestones

  • Published - 05/22/2018

Publication status

Published - 05/22/2018

ISSN

1470-269X

Publication IDs

  • Scopus: 85039424783
  • PubMed: 29205207
  • ORCID: /0000-0002-8636-1071/work/68811216

Publication metrics

Metrics

SciVal
citations
10
Fractional count
1
Fractional count
0.05
Fractional count
19
Fractional count
0.95
Fractional count
1
Fractional count
1
SciVal
FWCI
0.89
SciVal
Author count
20
SciVal
Paper percentile
81
Scopus
citations

PlumX, opens in new tab

Captures
41
Mentions
2
Citation count
28

Funding Details

FundersFunding numbers
NIAID
ZIGAI001048
JSPS
15K14983, 17K08383