Evidence map›Paper›PMID 26024286›Full record

ArticleBlood cancer journal2015

A novel antibody-drug conjugate targeting SAIL for the treatment of hematologic malignancies.

S Y Kim, J-W Theunissen, J Balibalos, S Liao-Chan, M C Babcock, T Wong, B Cairns, D Gonzalez, E H van der Horst, M Perez and 11 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 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
3.0field-weighted citation impact, top 10% 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, 17 citations in OpenAlex.

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  11. Multiple myeloma in the marrow: pathogenesis and treatments.Annals of the New York Academy of Sciences · 2016
    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

21 authors at 1 institution in 1 country.

S Y KimDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
J-W TheunissenDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
J BalibalosDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
S Liao-ChanDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
M C BabcockDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
T WongDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
B CairnsDepartment of Preclinical Development, Igenica Biotherapeutics, Burlingame, CA, USA.
D GonzalezDepartment of Preclinical Development, Igenica Biotherapeutics, Burlingame, CA, USA.
E H van der HorstDepartment of Preclinical Development, Igenica Biotherapeutics, Burlingame, CA, USA.
M PerezDepartment of Preclinical Development, Igenica Biotherapeutics, Burlingame, CA, USA.
Z LevashovaDepartment of Preclinical Development, Igenica Biotherapeutics, Burlingame, CA, USA.
L ChinnDepartment of Preclinical Development, Igenica Biotherapeutics, Burlingame, CA, USA.
J A D'AlessioDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
M FloryDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
A BermudezDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
D Y JacksonDepartment of Chemistry, Igenica Biotherapeutics, Burlingame, CA, USA.
E HaDepartment of Chemistry, Igenica Biotherapeutics, Burlingame, CA, USA.
J MonteonDepartment of Process Development, Igenica Biotherapeutics, Burlingame, CA, USA.
M F BruhnsDepartment of Process Development, Igenica Biotherapeutics, Burlingame, CA, USA.
G ChenDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
T-S MigoneDepartment of Biology, Igenica Biotherapeutics, Burlingame, CA, USA.
Juvaris BioTherapeutics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although several new therapeutic approaches have improved outcomes in the treatment of hematologic malignancies, unmet need persists in acute myeloid leukemia (AML), multiple myeloma (MM) and non-Hodgkin's lymphoma. Here we describe the proteomic identification of a novel cancer target, SAIL (Surface Antigen In Leukemia), whose expression is observed in AML, MM, chronic lymphocytic leukemia (CLL), diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL). While SAIL is widely expressed in CLL, AML, MM, DLBCL and FL patient samples, expression in cancer cell lines is mostly limited to cells of AML origin. We evaluated the antitumor activity of anti-SAIL monoclonal antibodies, 7-1C and 67-7A, conjugated to monomethyl auristatin F. Following internalization, anti-SAIL antibody-drug conjugates (ADCs) exhibited subnanomolar IC50 values against AML cell lines in vitro. In pharmacology studies employing AML cell line xenografts, anti-SAIL ADCs resulted in significant tumor growth inhibition. The restricted expression profile of this target in normal tissues, the high prevalence in different types of hematologic cancers and the observed preclinical activity support the clinical development of SAIL-targeted ADCs.

Indexed as

AminobenzoatesAnimalsAntibodies, MonoclonalAntigens, NeoplasmAntineoplastic AgentsChromatography, LiquidEnzyme-Linked Immunosorbent AssayFlow CytometryHematologic NeoplasmsHumansImmunotherapyIn Situ HybridizationMiceMice, SCIDOligopeptidesTandem Mass SpectrometryAminobenzoatesAntibodies, MonoclonalAntigens, NeoplasmAntineoplastic AgentsauristatinOligopeptides

Identifiers

PMID26024286
PMCPMC4476018
OpenAlexW1587404401

What OpenQuestion holds

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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.