Cancer stem cell niche as a therapeutic target

by Alexey Bersenev on December 27, 2009 · 1 comment

in cancer stem cell, niche

I wrote about a potential of therapeutic targeting so-called “cancer stem cell niche” while ago. I was always interested in role and potential targeting of leukemia-initiating cells microenvironment in bone marrow. Because of some new data came out of ASH annual meeting, I decided to keep you updated. I summarize the most interesting current and previous findings in leukemic stem cell niche targeting in the table below.

Basically, targeting of cancer stem cell environment focus on few mechanisms – adhesion and mobilization, cell cycle, hypoxia and angiogenesis.

Although the full nature of LIC-niche interaction remains elusive, it has been postulated as a useful target for leukemia therapy based on a dual rationale: on one hand, the survival of LICs may depend upon interactions with specific niche, while on the other hand, chasing LICs out of the BM niche may drive quiescent LICs into active cell cycle, sensitizing them for conventional chemotherapy.

The top part of table represent new targets, reported this year. The low part represent “old targets”. some of which have entered clinical trials.

potential agent
CASIN Cdc42 GTPase, selective mobilization of leukemia-initiating cells
ASH’09 abstract
PR-104 HIF-1α under hypoxia, reduced to hydroxylamine and amine metabolites that in turn induce DNA cross-links and cell death ASH’09 abstract
BBGC Glo-1 disrupt glycolysis in hypoxia-adapted quiescent leukemic cells
ASH’09 abstract
AMD3465 and
AMD3100 (Mozobil)
CXCR4 blocking LSC homing to a BM niche, mobilize and/or sensitizing leukemic cells to chemotherapy Blood 2009;113:6215

Blood 2009; 113:6206

LY294002 or QLT0267 integrin-linked kinase (ILK) inhibition of stroma-induced phosphorylation of Akt and GSK3β and other signaling pathways Cancer Res 2007;67:684
bevacizumab (anti-VEGF antibody) VEGF binding and inactivation of VEGF Clin Cancer Res 2004;10:3577
anti-VLA4 antibody VLA-4 Interrupt adhesion of leukemic cells to stromal cells
Nat Med 2003;9:1158
anti-CD44 antibody CD44 Interrupt adhesion of leukemic cells to niche cells Nat Med 2006;12:1167

One thing I didn’t get – How leukemic stem cell niche withing bone morrow in one hematological malignancy could be hypoxic and vascular in the same time? Let’s say if AML stem cells survival highly depends on hypoxia, targeting of this mechanism could succeed, but not targeting of vascularisation/angiogenesis.

Also read: The leukemic stem cell niche: current concepts
New insights into leukemic microenvironment in bone marrow
Therapeutic targeting of microenvironmental interactions in leukemia: Mechanisms and approaches

Connotea tags: cancer stem cell niche

{ 1 comment… read it below or add one }

Joanna December 27, 2009 at 11:56 pm

A little irrelevant, there’s a recent article that discusses how HIF2 is a central axis common to many tumor types ( Seems like drugs that target this TF will be particularly potent. HIF2 is of course differentially expressed from HIF1. I don’t have a lot of knowledge about HIF1. Is HIF1 a common axis in blood disorders? If so, it’s a better target than others for drug development.


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