Cancer is a highly complex disease caused by a set of oncogenic protein-coding genes and non-coding genes, and, thus, targeted analyses of these genes through highly innovative technologies are the best methods for cancer diagnosis, prognosis, risk assessment and treatment follow-up of various cancers. These are the most powerful research technologies that can save the lives of millions of cancer patients.
At GeneVerify, Inc., we have assembled a highly talented, multi-disciplinary team of molecular biologists, cell biologists, pathologists, biochemists, urologists, surgical oncologists, medical oncologists, radiation oncologists, physicians and surgeons committed every day to meeting the challenges of evolving gene-based diagnosis and treatment of various solid tumors.
GeneVerify, Inc., is developing in vitro diagnostic (IVD) reagents for laboratory- based assays for analysis of a set of oncogenic genes in various cancers using real-time PCR technology. We are also developing novel technologies to target these genes that will provide the most effective and highly specific treatment for various cancers.
(Protein coding genes and Non-coding genes analyses)
Analyses of a set of oncogenic protein coding genes and non-coding genes for in vitro diagnostic assays in research laboratory only. Analyses must be corelated by surgical oncologists/ medical oncologists/ radiation oncologists / pathologists/ physicians/ surgeons/ for diagnosis, prognosis, risk assessment and monitoring therapies of various cancers
In Vitro Diagnostic Reagents (Research and Development)
Targeting Oncogenic Protein coding genes and non-coding genes for treatment. Pre- IND (Investigational New Drug)
Genes based therapies that target oncogenes that are involved in cancer initiation, progression and metastasis.
Research and Development
Pre-IND (Investigational New Drug
Phase-1 Phase-2 Phase-3
“Precision Medicine” is a relatively new approach for disease treatment that takes into account, among other things, individual variability of genes. The precision medicine approach is based on genetic profiling of a set of tumors. Based on published literature, one in five patients that are newly diagnosed with cancer has a different combination of genetic changes and gene profiling, and, thus, one drug does not fit all with less consideration of the genetic differences between individuals. Therefore, each patient’s tumor has unique, individualized, genetic abnormalities, such as mutation, re-arrangement, translocation, polymorphic variants, gene fusions, gene amplification, gene deletion, abnormalities in microRNAs (miRNAs) and long-non-coding RNAs (lncRNAs), and DNA methylation.
In precision medicine, we must utilize the latest technologies for tumor genomics through multi-omics, such as genome, proteome, transcriptome, epigenome, metabolome, and microbiome profiling. Based on the Human Genome Project data analyses, there are more than 30,000 protein-coding genes and 60,000 non-coding genes.
Our professionals have dedicated their careers addressing cancer genetics and epigenetics for over 40 years and published more than 400 peer-reviewed research papers in high impact journals.
According to the NIH RePORTER database, our laboratory has been awarded / funded research projects 99 times through the NCI/NIH and U.S. Department of Veterans Affairs. We have several US patents in the field of urology and oncology resulting from major NCI/NIH funding initiatives.
At GeneVerify, Inc., we are developing in vitro diagnostic reagents for research laboratory- based assays for analysis of a set of oncogenes in various cancers using real-time PCR technology. We are also developing novel medical technologies to target these oncogenes that will provide the most effective and highly specific treatment for various cancers. These are the most powerful research and innovative technologies that can save the lives of millions of cancer patients.
According to the Human Genome Project data analyses, only 2% of the human genome is made up of protein-coding genes and 98% is comprised of non-coding genes. Based on the published literature and National Human Genome Research Institute data, there are about 30,000 protein-coding genes and about 60,000 non-coding genes.
We have identified a set of oncogenic protein-coding genes and non-coding genes that are the drivers for cancer initiation, progression and metastasis. Recent studies have shown that non-coding genes, such as microRNAs (miRNAs) and long-non-coding RNAs (lncRNAs), are involved in regulation of protein-coding genes through direct binding to the 3’UTR of oncogenes or RNA-RNA interactions. We hypothesize that analyses of a set of oncogenic protein-coding genes and non-coding genes are the most promising genetic biomarkers for cancer diagnosis, prognosis, and treatment follow-up.
According to the Cancer Statistics in 2022, about 20 million people worldwide are newly diagnosed with cancer every year in the world and, by 2030, this number is projected to be doubled if not controlled. The major problem is the lack of testing for early diagnosis, prognosis and monitoring of treatment follow-up. In some South East Asian countries, such as India, about 40% of cancer patients are metastatic at the time of diagnosis due to lack of testing. Almost all cancer patients die of metastasis and, presently, there is no effective therapy for metastatic cancer. Our professionals at GeneVerify, Inc., believe it is crucial to early identification and intervention that targeting a set of oncogenes can inhibit cancer progression and metastasis. These state of the art technologies will thereby improving patient outcomes while, at the same time, lowering healthcare costs.
Precision medicine is based on genetic profiling of a set of tumors. Based on the published literature, one in five patients that are newly diagnosed have different genetic profiling and, thus, one drug does not fit all. Therefore, gene-based diagnosis and therapy will absolutely transform and revolutionize the field.
Based on the published literature, about 35% of cancer patients that are normal by histology and clinical assessment have, in fact, early stage cancer based on their genetic profile. Our team of scientists at GeneVerify are developing innovative, gene-based testing for early diagnosis, prognosis and monitoring treatment, as well as gene-based treatments for various cancers.
We have assembled a highly talented team of molecular biologists, cell biologists, biochemists, pathologists, urologists, surgical oncologists, medical oncologists, radiation oncologists, physicians and surgeons that will address the gene-based diagnosis and treatment of various solid tumors.
We rationalize that altered expression of these sets of oncogenic protein- coding genes and non- coding genes can be used for early diagnosis, prognosis, risk assessment of individualized therapeutic intervention, and treatment follow-up for various cancers. We expect that targeting these genes will revolutionize the treatment of these cancers. These are the most powerful research technologies that can save the lives of millions of people.
GeneVerify, Inc., provides in vitro diagnostic reagents for research laboratory-based assays for analysis of sets of these oncogenic protein-coding and non-coding genes in various cancers. Our extensive network of colleagues is committed to developing novel technologies to target these genes with the goal to provide the path to the most effective and highly specific, individualized, treatment for various cancers. GeneVerify’s targeted genetic testing kits are the path to value-based rapid testing, discovery and identification, and risk prediction that is invaluable to early intervention.
Backed by our genetic testing profiling, medical oncologists and surgical oncologists may enable to (i) diagnose early stage cancer (ii) predict whether tumor is aggressive or slow growing and thus provide better decisions for surgery or active surveillance (iii) predict prognosis and risk assessment of cancer based on genetic profiling (iv) better predict how a patient might respond to certain modalities and therapies more accurately, and (v) achieve a solid basis for better decision-making on a patient’s therapeutic treatment and future evaluation to yield the quickest results, thereby enhancing your patient’s health, lengthen life, and reduce illness and disability.
At GeneVerify, Inc., we are tackling the issues that matter most to patient care in a collaborative setting where teamwork and innovation leads to more answers.
Founder, CEO and President
Chief Scientific Officer
Scientific Adviser
Kulkarni P, Dasgupta P, Hashimoto Y, Shiina M, Shahryari V, Tabatabai ZL, Yamamura S, Tanaka Y, Saini S, Dahiya R, Majid
Cancer Res. 2021 Mar 15;81(6):1500-1512. doi: 10.1158/0008-5472.CAN-20-0832. Epub 2021 Jan 26.PMID: 33500248.
Dasgupta P, Kulkarni P, Majid S, Hashimoto Y, Shiina M, Shahryari V, Bhat NS, Tabatabai L, Yamamura S, Saini S, Tanaka Y, Dahiya R.
Cell Death Dis. 2020 Aug 19;11(8):660. doi: 10.1038/s41419-020-02877-0.PMID: 32814766 Free PMC article.
Bhagirath D, Liston M, Patel N, Akoto T, Lui B, Yang TL, To DM, Majid S, Dahiya R, Tabatabai ZL, Saini S.
Oncogene. 2020 Dec;39(49):7209-7223. doi: 10.1038/s41388-020-01493-8. Epub 2020 Oct 9.PMID: 33037409 Free PMC article.
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