Clinical and Immunologic Characteristics of Colorectal Cancer Tumors Expressing LY6G6D.
Adrián Sanvicente GarcíaManuel PedregalLucía Paniagua-HerranzCristina Díaz-TejeiroCristina Nieto-JiménezPedro Pérez SeguraGyöngyi MunkácsyBalázs GyőrffyEmiliano CalvoVictor MorenoAlberto OcañaPublished in: International journal of molecular sciences (2024)
The identification of targets that are expressed on the cell membrane is a main goal in cancer research. The Lymphocyte Antigen 6 Family Member G6D ( LY6G6D ) gene codes for a protein that is mainly present on the surface of colorectal cancer (CRC) cells. Therapeutic strategies against this protein like the development of T cell engagers (TCE) are currently in the early clinical stage. In the present work, we interrogated public genomic datasets including TCGA to evaluate the genomic and immunologic cell profile present in tumors with high expression of LY6G6D . We used data from TCGA, among others, and the Tumor Immune Estimation Resource (TIMER2.0) platform for immune cell estimations and Spearman correlation tests. LY6G6D expression was exclusively present in CRC, particularly in the microsatellite stable (MSS) subtype, and was associated with left-side tumors and the canonical genomic subgroup. Tumors with mutations of APC and p53 expressed elevated levels of LY6G6D. This protein was expressed in tumors with an inert immune microenvironment with an absence of immune cells and co-inhibitory molecules. In conclusion, we described clinical, genomic and immune-pathologic characteristics that can be used to optimize the clinical development of agents against this target. Future studies should be performed to confirm these findings and potentially explore the suggested clinical development options.
Keyphrases
- copy number
- poor prognosis
- healthcare
- stem cells
- binding protein
- emergency department
- mental health
- squamous cell carcinoma
- gene expression
- small molecule
- protein protein
- induced apoptosis
- clinical trial
- neoadjuvant chemotherapy
- signaling pathway
- current status
- mesenchymal stem cells
- big data
- transcription factor
- rna seq
- cell cycle arrest
- pi k akt
- genome wide identification