2014
DOI: 10.1158/1538-7445.am2014-4189
|View full text |Cite
|
Sign up to set email alerts
|

Abstract 4189: Discovery of a novel carcinoma-associated EF hand containing protein by mining the dark matter of the human proteome

Abstract: The human genome contains thousands of novel and uncharacterized proteins. These unknown genes are difficult to mine due to lack of adequate information. Hence, they remain largely untapped. Reasoning that new druggable targets for cancer can be discovered from these uncharacterized proteins, we have developed a protocol to mine these proteins for cancer relevance. Using various cancer-related databases, we have developed a database of uncharacterized ORF proteins. Numerous ORFs from this database offer drugga… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
2
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(3 citation statements)
references
References 0 publications
0
2
0
Order By: Relevance
“…PPP1R17 is a member of an open reading frame that has been found to be associated with multiple solid tumors, including colorectal [ 34 ] and lung cancer [ 35 ]. Its HR is greater than 1 in this study indicating that it is a carcinogenic factor.…”
Section: Discussionmentioning
confidence: 99%
“…PPP1R17 is a member of an open reading frame that has been found to be associated with multiple solid tumors, including colorectal [ 34 ] and lung cancer [ 35 ]. Its HR is greater than 1 in this study indicating that it is a carcinogenic factor.…”
Section: Discussionmentioning
confidence: 99%
“…To date, a few numbers of public neoantigens have been recognized, whereas the private neoantigens usually originate from non-recurrent driver/passenger mutations and comprise most of the known neoantigens [25,26,54,[93][94][95][96]. Furthermore, based on the source from which the antigen is derived, the antigen can be canonical (derived from the protein-coding genes), or non-canonical (derived from nonprotein coding genes); in the canonical antigen, the antigen is expressed within the open reading frames (ORFs) of the protein-coding genes [93], such as the overexpression of numerous cancer-related genes [60,65,94], including p53 [97][98][99][100], cancer/testis antigens (CTAs) [100,101], and the human telomerase reverse transcriptase [102,103]. Non-canonical antigens are expressed outside of the ORFs [104], and can stem from alterations of the antigen at various levels, such as genomic, epigenomic, proteomic, transcriptomic, translational, and antigen-processing levels (intronic retention, alternative splicing, codon read-through, and noncanonical/non-AUG translation initiation levels) [93,100,105].…”
Section: Tumor Antigen Classificationsmentioning
confidence: 99%
“…Long read sequencing allows for detection of large structural variants and provides improved resolutions of haplotypes near tumor peptide-generating sequences of interest. Other technologies, such as ribosome profiling (Ribo-seq), will not only improve current tumor antigen predictions by confirming translation reading frames, but can open new tumor antigen sources, such as “genomic dark matter” arising from non-canonical reading frames ( Delgado et al 2014 ). We consider the version of LENS presented here to be a snapshot of the continuously improving workflow that will aid the immuno-oncology community toward improved therapeutics.…”
Section: Landscape Of Effective Neoantigens Softwarementioning
confidence: 99%