Evidence map›Paper›PMID 24119559›Full record

ArticleBioorganic & medicinal chemistry letters2013

Design, synthesis, and biological evaluation of bone-targeted proteasome inhibitors for multiple myeloma.

Joseph K Agyin, Bindu Santhamma, Sudipa S Roy

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Article
  2. Engineering small-molecule and protein drugs for targeting bone tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  3. Bone-Targeted Bortezomib Inhibits Bortezomib-Resistant Multiple Myeloma in Mice by Providing Higher Levels of Bortezomib in Bone.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  4. Review
  5. Bisphosphonates for delivering drugs to bone.British journal of pharmacology · 2021
    Review
  6. Review
  7. Review
  8. Review
  9. Targeting Bortezomib to Bone Increases Its Bone Anabolic Activity and Reduces Systemic Adverse Effects in Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2020
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. A review of molecular events of cadmium-induced carcinogenesis.Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer · 2014
    Review
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

3 authors.

Joseph K AgyinUniversity of Texas Health Science Center at San Antonio, Biochemistry Department, 7703 Floyd Curl Drive, San Antonio, TX 78229, United States; University of Texas Health Science Center at San Antonio, Cellular and Structural Biology Department, 7703 Floyd Curl Drive, San Antonio, TX 78229, United States. Electronic address: agyinj@uthscsa.edu.
Bindu Santhamma
Sudipa S Roy

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
Bone-seeking proteasome inhibitors for myelomaK01CA113468 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AGYIN, JOSEPH KOFI · 2005 to 2009
$728k
Novel targeted therapeutics for multiple myelomaR21CA153155 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AGYIN, JOSEPH KOFI · 2011 to 2014
$496k
NCI NIH HHS K01 CA113468NCI NIH HHS P30 CA054174NCI NIH HHS R21 CA153155
6 · The paper itself

Abstract

Multiple myeloma (MM) is an incurable neoplasm characterized by devastating and progressive bone destruction. Standard chemotherapeutic agents have not been effective at significantly prolonging the survival of MM patients and these agents are typically associated with often severe, dose-limiting side effects. There is great need for methods to target the delivery of novel, effective cytotoxic agents specifically to bone, where myeloma cells reside. We have synthesized and evaluated the effects of the bone-targeted proteasome inhibitors PS-341-BP-1, PS-341-BP-2 and MG-262-BP on cell proliferation using the mouse 5TGM1 and human RPMI 8226 cell lines in vitro. The compounds exhibit strong cytotoxicity on MM cell lines and reduce the number of viable cells in a dose dependent manner.

Indexed as

AnimalsAntineoplastic AgentsBone and BonesBone Density Conservation AgentsBoronic AcidsCell Line, TumorCell ProliferationDiphosphonatesHumansMiceMultiple MyelomaProteasome InhibitorsAntineoplastic AgentsBone Density Conservation AgentsBoronic AcidsDiphosphonatesProteasome InhibitorsBisphosphonate conjugateBone-targetedBoronic acidMultiple myelomaProteasome inhibitor

Identifiers

PMID24119559
PMCPMC3836429

What OpenQuestion holds

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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.