Recent Patents on DNA & Gene Sequences

ISSN: 1872-2156

Recent Patents on DNA & Gene Sequences
Volume 1, Number 1, February 2007


Contents



Advanced Nanotechnological Approaches for Designing Protein-Based “Lab-on-Chips” Sensors on Porous Silicon Wafer Pp. 1-7
Stefano Borini, Maria Staiano, Massimiliano Rocchia, Andrea M. Rossi, Mose Rossi, and Sabato D’Auria
[Abstract] [Full Text Article]


Recent Patents of Gene Sequences Relative to the Phosphatidylinositol 3-kinase / Akt Pathway and their Relevance to Drug Discovery Pp. 9-23
Kathrin T. Doepfner, Danielle Boller, Angela De Laurentiis, Ana S. Guerreiro, Marin Marinov and Alexandre Arcaro
[Abstract] [Full Text Article]


Patenting Human Genes and Stem Cells Pp. 25-34
Enca Martin-Rendon and Derek J. Blake
[Abstract] [Full Text Article]


Recent Patents Relating to Tumor Suppressor Genes Pp. 35-41
Jason J. Derry and Yijan E. Chang
[Abstract] [Full Text Article]


Modulating Mitochondria-Mediated Apoptotic Cell Death Through Targeting of Bcl-2 Family Proteins Pp. 43-61
Abdel Aouacheria, Agnès Cibiel, Yannis Guillemin, Germain Gillet and Philippe Lalle
[Abstract] [Full Text Article]


The Importance of Bio-Computational Tools for Predicting HIV Drug Resistance Pp. 63-68
Antonio Carvajal-Rodríguez
[Abstract] [Full Text Article]


Current and Future Developments in Patents for Quantitative Trait Loci in Dairy Cattle Pp. 69-76
Joel I. Weller
[Abstract] [Full Text Article]


Patent Annotations Pp. 77-80

Patent Selections
Pp. 81-93




Abstracts


[Back to top]
Advanced Nanotechnological Approaches for Designing Protein-Based “Lab-on-Chips” Sensors on Porous Silicon Wafer

Stefano Borini, Maria Staiano, Massimiliano Rocchia, Andrea M. Rossi, Mose Rossi, and Sabato D’Auria

[Full Text Article]

In this article, we will review the more recent patented approaches related to the design and development of micro- and nano-patterns of biomolecules on solid substrates for the realization of innovative biochips, including inkjet and spotting technology, and Scanning Probe Methods In addition, we will report on some important patents based on the use of porous materials as substrates, exploiting the large specific surface for the design of highly sensitive biodevices. The main advantages and drawbacks related to each technological approach to the biochips fabrication will be pointed out, and future perspectives in the field will be discussed.


[Back to top]
Recent Patents of Gene Sequences Relative to the Phosphatidylinositol 3-kinase / Akt Pathway and their Relevance to Drug Discovery
Kathrin T. Doepfner, Danielle Boller, Angela De Laurentiis, Ana S. Guerreiro, Marin Marinov and Alexandre Arcaro

[Full Text Article]

Phosphoinositide 3-kinases (PI3Ks) play an essential role in the signal transduction events initiated by the binding of extracellular signals to their cell surface receptors. There are eight known PI3Ks in humans, which have been subdivided into three classes (I-III). The class IA of PI3K comprises the p110α, p110β and p110δ isoforms, which associate with receptor tyrosine kinases (RTKs). On the other hand, the class IB PI3K p110γ is regulated by G-protein-coupled receptors (GPCRs). Gene targeting studies in mice have revealed specific biological functions for the class IA p110δ in lymphocyte activation, and the class IB p110γ in inflammatory cell responses. In human cancer, recent reports have described activating mutations in the PIK3CA gene encoding p110α, and inactivating mutations in the PTEN gene, a tumor suppressor and antagonist of the PI3K pathway. Thus, individual PI3K isoforms are potential drug targets for a variety of human diseases, including allergies, cancer, rheumatoid arthritis and arterial thrombosis. In this review, we will discuss recent patents relating to class I PI3Ks, including patents on the cDNA sequences of p110γ and p110δ. Moreover, we will review patents on novel pharmacological PI3K inhibitors and on methods of manipulating T cell responses through PI3K.


[Back to top]
Patenting Human Genes and Stem Cells
Enca Martin-Rendon and Derek J. Blake

[Full Text Article]

Cell lines and genetically modified single cell organisms have been considered patentable subjects for the last two decades. However, despite the technical patentability of genes and stem cell lines, social and legal controversy concerning their ‘ownership’ has surrounded stem cell research in recent years. Some granted patents on stem cells with extremely broad claims are casting a shadow over the commercialization of these cells as therapeutics. However, in spite of those early patents, the number of patent applications related to stem cells is growing exponentially. Both embryonic and adult stem cells have the ability to differentiate into several cell lineages in an organism as a result of specific genetic programs that direct their commitment and cell fate. Genes that control the pluripotency of stem cells have been recently identified and the genetic manipulation of these cells is becoming more efficient with the advance of new technologies. This review summarizes some of the recent published patents on pluripotency genes, gene transfer into stem cells and genetic reprogramming and takes the hematopoietic and embryonic stem cell as model systems.


[Back to top]
Recent Patents Relating to Tumor Suppressor Genes
Jason J. Derry and Yijan E. Chang

[Full Text Article]

Researchers in the field of tumor suppressor genes are actively attempting to discover new tumor suppressor genes and/or characterize known tumor suppressor genes with the intention of treating and diagnosing cancers. A number of recent patents and patent applications have been published that discuss some of these discoveries. Some of the patents and patent applications discuss newly discovered tumor suppressor genes, including WW Domain-Containing Oxidoreductase (WWOX), Cancer Associated Ring-1 (CAR-1), Human Cervical Cancer Suppressor 1 (HCCS-1), Src-suppressed C kinase substrate (SSeCKS), ADP-Ribosylation factor-like putative Tumor Suppressor gene 1 (ARTS1), and Deleted in Osteosarcoma (DOS). One Recent Patent describes the discovery that known caspase family member caspase-8 (CASP8) is a tumor suppressor. Another Recent Patent describes the use of Wilms Tumor suppressor gene (WT1) peptides as a cancer vaccine. In addition, Sakai et al. received a patent describing a fragment of the p51 tumor suppressor gene containing a promoter region, which is useful for identifying compounds that modulate p51 activity. Another patent application recently published describes a chimeric tumor suppressor gene generated by combining a portion of the rat PEG-3 protein with the human GADD34 protein, thus creating a protein with apoptotic activity. These patents and patent applications provide valuable information that may be useful in fighting cancer by focusing on tumor suppressor gene activities.


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Modulating Mitochondria-Mediated Apoptotic Cell Death Through Targeting of Bcl-2 Family Proteins
Abdel Aouacheria, Agnès Cibiel, Yannis Guillemin, Germain Gillet and Philippe Lalle

[Full Text Article]

Research demonstrated that the function of mitochondria extends well beyond that of being cell powerhouses and revealed that these organelles fulfil a dual role in both cellular life and death. In most vertebrates, execution of the mitochondrial pathway of apoptosis requires permeabilization of the mitochondrial outer membrane, an event which allows for the release of a variety of intramembrane space proteins, leading to the activation of caspases and ultimately cell demise. Bcl-2 family proteins, which include pro- and antiapoptotic members, positively or negatively regulate mitochondrial outer membrane permeabilization, i.e. a barrier to apoptosis induction. Over-expression of Bcl-2 and Bcl-xL is associated with tumor progression and may be responsible for drug resistance, making pro-survival Bcl-2 family members important targets for the development of anticancer agents. Pharmacological apoptosis modulation by manipulation of pro-apoptotic Bcl-2 family proteins, with the goal to treat disorders associated with uncontrolled cell death or to kill unwanted cells, is likely to represent an additional research focus in the coming years. The purpose of this review is to describe, with examples taken from recent patents, novel strategies for targeting the Bcl-2 family of apoptotic regulators through peptide-based approaches and selective delivery of functional nucleic acids.


[Back to top]
The Importance of Bio-Computational Tools for Predicting HIV Drug Resistance
Antonio Carvajal-Rodríguez

[Full Text Article]

The battle against retrovirus HIV-1 has reached a critical point. Antiretroviral resistance appears under highly active anti-retroviral therapy and the use of new drug combinations capable to overcome the emerged resistance is necessary. After detecting drug resistance two main approaches are possible. The phenotypic assays study in vitro the replication ability of virus variants in the presence or absence of drugs. This approach is expensive and time consuming. The genotypic assays try to obtain information from viral sequences coding for the drug targets in order to detect mutations with low susceptibility to drugs. Although this approach is faster and cheaper, a clear interpretation of the results is not always possible. In this work, I comment and analyze some new patents that point towards more efficient resistance detection and integral data management and prediction systems performing an efficient personalized combined therapy. In the future, computational tools will be essential as exploratory and interpretation systems in order to obtain a better support of clinical decisions concerning both the prediction and the evolution of drug resistance. Importantly, the revised patents conform to this trend.


[Back to top]
Current and Future Developments in Patents for Quantitative Trait Loci in Dairy Cattle
Joel I. Weller

[Full Text Article]

Many studies have proposed that rates of genetic gain in dairy cattle can be increased by direct selection on the individual quantitative loci responsible for the genetic variation in these traits, or selection on linked genetic markers. The development of DNA-level genetic markers has made detection of QTL nearly routine in all major livestock species. The studies that attempted to detect genes affecting quantitative traits can be divided into two categories: analysis of candidate genes, and genome scans based on within-family genetic linkage. To date, 12 patent cooperative treaty (PCT) and US patents have been registered for DNA sequences claimed to be associated with effects on economic traits in dairy cattle. All claim effects on milk production, but other traits are also included in some of the claims. Most of the sequences found by the candidate gene approach are of dubious validity, and have been repeated in only very few independent studies. The two missense mutations on chromosomes 6 and 14 affecting milk concentration derived from genome scans are more solidly based, but the claims are also disputed. A few PCT in dairy cattle are commercialized as genetic tests where commercial dairy farmers are the target market.

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