Identification
and validation
of new therapeutic
targets



Helios Biosciences - Target Designer

Our R&D Program
Prostate Cancer
Immuno-dyn

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European Projects
Valapodyn (Website, Brochure)
Tempo (Website)
Inflacare (Website)

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Helios BioSciences
102, avenue Gaston Roussel
93230 Romainville
France
Phone : +33 (0)157 148 396
Fax : +33 (0)972 314 803
Contact




Selection of Therapeutic Targets for Prostate Cancer by using the Dynamic Modeling technology of Helios BioSciences: APO-KDYN.

Context:

Currently, prostate cancer is the most frequently diagnosed cancer in men. The risk of developing prostate cancer increases with age and 30 men in 100 aged 50 years or more will develop prostate cancer. Approximately 3 in 10 men with prostate cancer will die from this illness and its complications. Generally speaking, chemotherapy is ineffective against prostate cancer and at present, treatments such as radiotherapy or total prostatectomy are used. The majority of prostate cancers are cancers of clinically hormone-sensitive secretory cells which are biologically androgen dependant. 95% are adenocarcinomas of which 50% are well defined glandular epitheliomas. One of the most frequently used therapeutic strategies for advanced cancers (1/3 of patients show metastases at diagnosis) consists of depriving cancer cells of androgens which has an atrophic effect on the cells, making them to evolve towards cell death notably by apoptosis. Unfortunately, a small number of cells escape treatment and can form more serious forms of the cancer long term. Prostate cancers with metastases generally respond to anti-androgen treatments only for 12 to 16 months, a duration which has notably not been improved for over than 15 years. Cancer cells which escape hormonal treatment are even more difficult to treat and average survival is of only 9-12 months. At this stage, chemotherapy is disappointing and badly tolerated. By way of example, in the recent evaluation of a bi-chemotherapy, the toxicity of the treatment caused it to be stopped prematurely in 49% of the patients and in spite of the aggressiveness of the protocol, average survival was only 44 weeks (11 months).

APO-KDYN Program:

Objectives

Taking these needs into account, the APO-KDYN project proposes a new therapeutic strategy for prostate cancer based on the acceleration of cancerous cell death during androgen deprivation in order to accelerate the reduction of the tumour mass and to reduce the appearance of cells resistant to androgen deprivation.

 

The major APO-KDYN objectives are :

  1. the creation of a mathematical dynamic model of prostatic cancerous cell death by Helios novel modeling technology
  2. the selection and the validation of new therapeutic targets to cure the prostate cancer.

June 2011

Meet us in Washington during BIO 2011. Visit us on our booth (hosted by the competitiveness bio-cluster Medicen) , request a meeting during the Bio Business Forum or attend the Fast-Track session organized by the French competitiveness clusters.

April 2011

Meet us in Boston during Bio-IT World Conference and Expo '11

October 2010

Helios discusses its technology during the 11th International Conference on System Biology in Edinburgh (Get a copy of our poster)

June 2010

A publication describing our technology and its use in an european community founded program (FP6: VALAPODYN): Pubmed 20459389.

May 2010

BIO 2010 : After attending BIoEurope Spring, we will attend BIO 2010 in Chicago. We will be happy to meet you at the French Pavillion (#3712) or during the Bio Business Forum.

March 2010

Immunosupressive drug targets : We have finalized the experimental validation of 3 of the 6 immunosupressive targets that we have selected. This confirms the immunosuppressive potential of these targets.

January 2010

Year 2009 overview


Testimonies
I warmly recommend resorting to Helios BioSciences for any operation of mRNA detection in the brain as well as in other tissues. Their professionalism, their know-how, their dynamism, their customer care and adaptability make them now indispensable collaborators."

Bruno Giros, PhD, Director of the INSERM Research Department U-513, "Neurobiology and Psychiatry"

The primary roadblock in exploring neuromuscular junctions is their relatively small size (~50nm). Helios has certainly shown that it is capable of overcoming barriers and exploring new grounds in science through dedication and persistence."

Javad Nazarian, M.S., The Children's National Medical Center, Washington DC.

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