M A Nezami
Pacific Medical Center of Hope, USA
Scientific Tracks Abstracts: J Cancer Sci Ther
There are several barriers that influence the effective treatment of solid tumors by conventional therapies. These barriers
include tumor heterogeneity and the genetic instability of cancer. It has been hypothesized that these problems may be
managed by targeting angiogenesis, as angiogenic signals modify the micro-environmental cross-talk by the tumor. Oncogenic
driver events may also influence the viability and clinical behavior of a given tumor. Some driver mutations are found to be
targets for therapy, whereas others play crucial roles in resistance to therapy. The challenge is that tumor cells have a very
sophisticated mechanism of survival, by switching their driving pathways and signaling transduction pathways in a dynamic
fashion. This understanding has prompted efforts aimed at treating tumor cells with multiple drugs to inhibit as many targets
as possible. The majority of these combination therapies have failed to be clinically advantageous. Research of epigenetic
regulations of these targets, including angiogenesis, is relevant and exciting. We present a summary of cases of advanced
Stage IV patients with heterogeneous cancer who were treated using a novel epigenetic therapy, in a protocol called multi
targeted epigenetic therapy (MTET), resulting in independent “antiangiogenic response”, as well as decreased heterogeneity
of tumors, and overall reduction of tumor burden. These reductions were measured by serum/plasma VEGF measurements
as a biomarker for vasculogenesis, circulatory tumor DNA and by circulatory tumor cells analysis. These markers translated
to improved progression free or overall survival, and proved to be prognostic in many cases. We conclude that this small
sample presents considerable effect size, and may impact the current practice of oncology by providing better prognostic and
therapeutic tools targeting epigenetic aberrancies in refractory heterogeneous disease, by regulating the epigenome.
Nezami M, Hager S, Garner J (2016) The role of telomeres in cancer development and progression, and the double edge sword effect with tamoxifen. Biology and medicine 8:3.
Nezami M, Hager S, Garner J (2016) Preliminary findings on multi-targeted epigenetic therapy in modifying telomerase activity. Cancer science open access 2:1:007.
Nezami M, Hager S, Garner J (2016) Epigenetic tumor response to hypoxia: An epimutation pattern and a method of multi targeted epigenetic therapy (MTET). Journal of cancer therapy 254-269.
Nezami M A, Simon A G & Bartholomeusz G (2016) Correlation of an ex vivo model with clinical application of an epigenetic modifier, inhibiting tumor growth and metastasis, in resistant cholangiocarcinoma: A case study. Journal of cancer therapy 07(01) 50-54.
M A Nezami is a Board Certified Physician graduated from USC and UCSF residencies and fellowship and trained in Integrative Cancer Therapy. He serves as Researcher and national and international Speaker, in Oncology and Epigenetic field. He has been involved in many research projects and publications/presentations. He is an Inventor and Innovator and has designed a new method of treating advanced cancer, called Multi Molecular Targeted Epigenetic Therapy (MTET). With this method, over the last 7 years, he has successfully treated many patients, mostly with advanced cancer who had failed conventional methods.
Email: [email protected]