Antibody–drug conjugates as novel anti-cancer chemotherapeutics

C Peters, S Brown - Bioscience reports, 2015 - portlandpress.com
Over the past couple of decades, antibody–drug conjugates (ADCs) have revolutionized the
field of cancer chemotherapy. Unlike conventional treatments that damage healthy tissues …

[HTML][HTML] New developments for antibody-drug conjugate-based therapeutic approaches

BECG de Goeij, JM Lambert - Current opinion in immunology, 2016 - Elsevier
Highlights•Albeit their clinical success, ADCs have a relatively narrow therapeutic
index.•Dose-limiting toxicities of ADCs are frequently unrelated to the targeted …

Redox-directed cancer therapeutics: molecular mechanisms and opportunities

GT Wondrak - Antioxidants & redox signaling, 2009 - liebertpub.com
Redox dysregulation originating from metabolic alterations and dependence on mitogenic
and survival signaling through reactive oxygen species represents a specific vulnerability of …

Immunophenotyping of acute leukemia and lymphoproliferative disorders: a consensus proposal of the European LeukemiaNet Work Package 10

MC Béné, T Nebe, P Bettelheim, B Buldini, H Bumbea… - Leukemia, 2011 - nature.com
Abstract The European LeukemiaNet (ELN), workpackage 10 (WP10) was designed to deal
with diagnosis matters using morphology and immunophenotyping. This group aimed at …

Probing the biology of natural products: molecular editing by diverted total synthesis

AM Szpilman, EM Carreira - Angewandte Chemie International …, 2010 - Wiley Online Library
The systematic modification of natural products through diverted total synthesis is a powerful
concept for the systematic modification of natural products with the aim of studying …

Siglecs as positive and negative regulators of the immune system

PR Crocker, P Redelinghuys - Biochemical Society Transactions, 2008 - portlandpress.com
Siglecs (sialic acid-binding Ig-like lectins) are mainly expressed in the immune system. Sn
(sialoadhesin)(siglec-1), CD22 (siglec-2) and siglec-15 are well conserved, whereas the …

A recombinant trispecific single‐chain Fv derivative directed against CD123 and CD33 mediates effective elimination of acute myeloid leukaemia cells by dual …

M Kügler, C Stein, C Kellner, K Mentz… - British journal of …, 2010 - Wiley Online Library
Two trivalent constructs consisting of single‐chain Fv antibody fragments (scFvs) specific for
the interleukin‐3 receptor α chain (CD123), CD33 and the Fcγ‐receptor III (CD16) were …

[HTML][HTML] In Vitro Pre-Clinical Validation of Suicide Gene Modified Anti-CD33 Redirected Chimeric Antigen Receptor T-Cells for Acute Myeloid Leukemia

K Minagawa, MO Jamil, M Al-Obaidi, L Pereboeva… - PLoS …, 2016 - journals.plos.org
Background Approximately fifty percent of patients with acute myeloid leukemia can be
cured with current therapeutic strategies which include, standard dose chemotherapy for …

In Vitro and In Vivo Antitumor Effect of Anti‐CD33 Chimeric Receptor‐Expressing EBV‐CTL against CD33+ Acute Myeloid Leukemia

A Dutour, V Marin, I Pizzitola… - Advances in …, 2012 - Wiley Online Library
Genetic engineering of T cells with chimeric T‐cell receptors (CARs) is an attractive strategy
to treat malignancies. It extends the range of antigens for adoptive T‐cell immunotherapy …

The polyamine transport system as a target for anticancer drug development

AJ Palmer, HM Wallace - Amino acids, 2010 - Springer
The vast majority of anticancer drugs in clinical use are limited by systemic host toxicity due
to their non-specific side effects. These shortcomings have led to the development of tumour …