AEterna Zentaris (AEZS) Presents Positive Preclinical Data in Breast Cancer on AEZS-131, a Highly Selective Erk 1/2 Inhibitor, at San Antonio Breast Cancer Symposium
12/9/2011 7:11:24 AM
QUEBEC CITY, Dec. 9, 2011 /PRNewswire/ - Aeterna Zentaris Inc. (NASDAQ:
AEZS) (TSX: AEZ) (the "Company") today announced positive preclinical
data in triple-negative breast cancer (TNBC) for its highly selective
Erk 1/2 inhibitor anticancer compound, AEZS-131. Data showed that
AEZS-131 selectively inhibits Erk at low nanomolar (nM) concentrations
and induces G1 arrest. Accordingly, the cytotoxic effect of AEZS-131
was most pronounced in TNBC cell lines with mutations in the MAPK
pathway. Data were presented yesterday by Dr. Jörg B. Engel, Medical
University of Regensburg, Department of Gynaecology and Obstetrics,
Germany, during a poster session at the CTRC - AACR San Antonio Breast
Cancer Symposium, in San Antonio, Texas.
| Poster #P3-18-06: | "AEZS- 131 - a highly selective ERK-inhibitor: Characterization and
preclinical testing in triple-negative breast cancer (TNBC)", Engel Jörg B., Seipelt Irene, Hönig Arnd, Hahne Jens C., Teifel Michael.
|
The Study
AEZS-131 was tested to check for selectivity, inhibition of
Rsk-phosphorylation (cellular substrate of Erk), mode of action and
cleavage of PARP. Cytotoxic efficacy was evaluated in a selection of
TNBC cell lines, with or without mutations in the MAPK signal
transduction pathway, by MTT assay.
Results
The study showed that AEZS-131 selectively inhibited ERK with an IC50<4nM. Phosphorylation of Rsk-1, the cellular substrate of Erk, was
inhibited with an IC50 of 158 nM. AEZS-131 induced cell cycle arrest in G1 dose-dependently
and cleavage of PARP. EC50 values were below 1µM for cell lines with mutations in the MAPK
pathway. TNBC cell lines without mutations in the MAPK pathway were
less responsive.
Dr. Jörg B. Engel, of the Medical University of Regensburg, commented,
"Over-expression of MAPK has been detected in 34% of triple-negative
breast cancer and has been found to be associated with an increased
risk for recurrence in patients with this type of breast cancer. Since
preclinical data suggest that AEZS-131's cytotoxic effect was most
pronounced in triple-negative breast cancer cell lines with mutations
in the MAPK pathway, we, therefore, believe this compound should be
further explored in triple-negative breast cancer with over activation
of MAPK or mutations in the MAPK-pathway."
The poster is available at the following link.
About Erk 1/2 Inhibitor Compound
Extracellular signal-regulated kinases ("Erks") act in the
Ras-Raf-Mek-Erk signaling cascade and regulate various cellular
processes such as cell growth, proliferation and survival in response
to a variety of extracellular or intrinsically mutated upstream
signals. Aeterna Zentaris has identified small molecular compounds that
selectively inhibit Erk 1/2, among them AEZS-131, which has been shown
to significantly inhibit tumor growth in in vivo studies. Early development of the Erk inhibitor AEZS-131 is an integral
part of Aeterna Zentaris' kinase research program comprising the
investigation of different compounds for single Erk inhibition, single
PI3K inhibition and dual Erk/PI3K kinase inhibition.
About Aeterna Zentaris Inc.
Aeterna Zentaris is a late-stage oncology drug development company
currently investigating potential treatments for various cancers
including colorectal, multiple myeloma, endometrial, ovarian, prostate
and bladder cancer. The Company's innovative approach of "personalized
medicine" means tailoring treatments to a patient's specific condition
and to unmet medical needs. Aeterna Zentaris' deep pipeline is drawn
from its proprietary discovery unit providing the Company with constant
and long-term access to state-of-the-art therapeutic options. For more
information please visit www.aezsinc.com
Forward-Looking Statements
This press release contains forward-looking statements made pursuant to
the safe harbour provisions of the U.S. Securities Litigation Reform
Act of 1995. Forward-looking statements involve known and unknown risks
and uncertainties that could cause the Company's actual results to
differ materially from those in the forward-looking statements. Such
risks and uncertainties include, among others, the availability of
funds and resources to pursue R&D projects, the successful and timely
completion of clinical studies, the risk that safety and efficacy data
from any of our Phase 3 trials may not coincide with the data analyses
from previously reported Phase 1 and/or Phase 2 clinical trials, the
ability of the Company to take advantage of business opportunities in
the pharmaceutical industry, uncertainties related to the regulatory
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SOURCE AETERNA ZENTARIS INC.