20-F – Annual and transition report of foreign private issuers [Sections 13 or 15(d)]

(Filing, Annual, Can-Fite BioPharma, 2015, MAR 31, 2016, View Source [SID:1234510271])

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Telomerase reactivation in cancers: mechanisms that govern transcriptional activation of the wild-type versus mutant TERT promoters.

Transcriptional activation of telomerase reverse transcriptase (TERT) gene is a rate-limiting determinant in the reactivation of telomerase expression in cancers. TERT promoter mutations represent one of the fundamental mechanisms of TERT reactivation in cancer development. We review recent studies that elucidate the molecular mechanisms underscoring activation of mutant TERT promoters.

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Celator® Pharmaceuticals Announces New Data for VYXEOS™ in FLT3-ITD Mutated AML Cells Derived from Patients with Newly Diagnosed AML to be Presented at the American Association for Cancer Research Annual Meeting

On March 31, 2016 Celator Pharmaceuticals, Inc. (Nasdaq: CPXX) reported that data for VYXEOS (cytarabine:daunorubicin) Liposome for Injection (also known as CPX-351), its lead product candidate, will be presented at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting in New Orleans, LA, April 16-20, 2016 (Press release, Celator Pharmaceuticals, MAR 31, 2016, View Source [SID:1234510229]).

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The research was conducted in the laboratory of Dr. Jeffrey Tyner at Oregon Health & Science University. The objective of the research was to examine the ex vivo sensitivity of acute myeloid leukemia (AML) cells derived from newly diagnosed patients to VYXEOS. This work supports the observed clinical benefit of VYXEOS in high-risk AML patients and may provide a means of identifying patient genotypes/phenotypes most sensitive to VYXEOS.

"We continue to learn more about the unique activity of VYXEOS in AML and enhance our ability to match this performance with specific patient characteristics that could be predictive of improved outcomes," said Lawrence Mayer, Ph.D., President and Chief Scientific Officer at Celator. "The research being undertaken by Dr. Tyner reflects Celator’s goal to elucidate the clinical benefits of VYXEOS by expanding our scientific understanding of its mechanism of action, particularly in AML cells with important molecular phenotypes."

Details on the AACR (Free AACR Whitepaper) poster presentation:

Presentation Title:
CPX-351 cytotoxicity against fresh AML blasts is increased for FLT3-ITD+ cells and correlates with drug uptake and clinical outcomes
Date/Time:
Sunday, April 17, 2016 – 1:00pm-5:00pm
Session Category:
Poster Presentation
Session Title:
ET01-03, Combination Chemotherapy
Location:
New Orleans Convention Center, Halls G-J Poster Section 15
Abstract Number:
287

The poster will be available on Celator’s website (www.celatorpharma.com) at the conclusion of the AACR (Free AACR Whitepaper) meeting.

Scientists discover new way to tackle challenging children’s brain tumours

On March 31, 2016 Cancer Research UK reported that scientists have discovered why a curable type of children’s brain tumour is so responsive to chemotherapy – paving the way to improve treatment of tumours that are harder to tackle, according to research by a Cancer Research UK scientist published in Cancer Cell* (Press release, Cancer Research UK, MAR 31, 2016, View Source [SID:1234510278]).

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"This could make chemotherapy even more effective and reduce the amount of radiation that we give to children." – Professor Richard Gilbertson
This study shows that a curable type of brain tumour in children – called WNT medulloblastoma** – grows ‘leaky’ blood vessels that allow much higher than normal levels of chemotherapy drugs to reach the cancer cells.

Healthy blood vessels in the brain can filter potentially damaging molecules and prevent them from reaching brain tissue. But this can also restricts drugs from reaching tumour cells in the brain.

But in a tumour with leaky blood vessels, like certain types of medulloblastoma, these molecules cannot be kept out.

Understanding why curable tumours are easier to treat could help find more effective treatments for less curable types of medulloblastoma. For these patients, researchers think they might be able to turn this barrier off and make the tumours more responsive to chemotherapy.

Professor Richard Gilbertson, lead author who has recently joined Cancer Research UK’s Cambridge Institute, said: "This research is exciting because it means that as well as finding kinder treatments for a curable type of brain tumour, we may also be able to manipulate brain tumours that are difficult to treat successfully to make them more responsive to treatment.

"This could make chemotherapy even more effective and reduce the amount of radiation that we give to children. This would mean fewer long term side effects for children later in life which is something we’re always working towards."

Professor Pamela Kearns, Cancer Research UK’s children’s cancers expert, said: "This research gives us valuable insight into why some brain tumours respond better to chemotherapy than others. While cancer survival overall has doubled over the past 40 years, treatments for brain tumours have seen much slower progress. And brain tumours in children remain a major challenge.

"Cancer Research UK have made these challenges areas of priority and set up a specific Kids & Teens campaign to increase the investment in research focussed on children’s cancers. More research is needed to help us find ways to diagnose and treat the disease earlier and develop more effective treatments that have less of the long term side effects that can have a major impact throughout a child’s adult life."

This research was funded by ALSAC and the National Cancer Institute and carried out at St Jude Children’s Research Hospital.

Development of a Functional Biomarker for Use in Cell-Based Therapy Studies in Seropositive Rheumatoid Arthritis.

: Cell-based therapy has potential therapeutic value in autoimmune diseases such as rheumatoid arthritis (RA). In RA, reduction of disease activity has been associated with improvement in the function of regulatory T cells (Treg) and attenuated responses of proinflammatory effector T cells (Teff). Mesenchymal stem cells (MSCs) and related multipotent adult progenitor cells (MAPC) have strong anti-inflammatory and immunomodulatory properties and may be able to "reset" the immune system to a pre-RA state. MAPC are MSC-like cells that are slightly earlier in lineage, have greater expansion capacity, and can be used as "off-the-shelf" therapy. Assessment of cell-based therapy to treat arthritis and related diseases is limited by the lack of available biological correlates that can be measured early on and indicate treatment response. We set out to develop a functional measure that could be used ex vivo as a biomarker of response. We were able to demonstrate that MAPC products could inhibit Teff responses from patients with active RA and that Treg from RA patients suppressed Teff. This assay used ex vivo can be used with MAPC or Treg alone or in combination and reflects the overall level of Teff suppression. Use of a novel functional biomarker as an exploratory endpoint in trials of cell-based therapy should be of value to detect biological outcomes at a point prior to the time that clinical response might be observed.
Therapy with mesenchymal stem cells and related multipotent adult progenitor cells is immune modifying in a variety of diseases. There is interest in using cell-based therapy in rheumatoid arthritis (RA) to induce tolerance and "reset" the immune system to its pre-RA state. In a clinical trial, it should be known as soon as possible if there is a chance of response. A biomarker has been developed that permits measurement of the effects of cell-based therapy on effector T cell function.
©AlphaMed Press.

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