scispace - formally typeset
S

Sasha Lazetic

Researcher at OncoMed

Publications -  11
Citations -  4626

Sasha Lazetic is an academic researcher from OncoMed. The author has contributed to research in topics: Receptor & Natural killer cell. The author has an hindex of 10, co-authored 10 publications receiving 4281 citations. Previous affiliations of Sasha Lazetic include Maxygen.

Papers
More filters
Journal ArticleDOI

HLA-E binds to natural killer cell receptors CD94/NKG2A, B and C

TL;DR: The identification of ligands for HLA-E is reported, which shows that a subset of HLA class I alleles has been shown to inhibit killing by CD94/NKG2A+ NK-cell clones, and only the HLA alleles that possess a leader peptide capable of upregulating Hla-E surface expression confer resistance toNK-cell-mediated lysis.
Journal ArticleDOI

Colorectal cancer stem cells are enriched in xenogeneic tumors following chemotherapy.

TL;DR: Residual tumors are enriched in colon tumors following chemotherapy and remain capable of rapidly regenerating tumors from which they originated, thereby suggesting avenues for improving cancer therapy.
Journal ArticleDOI

Wnt pathway inhibition via the targeting of Frizzled receptors results in decreased growth and tumorigenicity of human tumors

TL;DR: A therapeutic approach to targeting the Wnt pathway with a monoclonal antibody, OMP-18R5, which interacts with five Fzd receptors through a conserved epitope within the extracellular domain and blocks canonical Wnt signaling induced by multiple Wnt family members.
Journal Article

Human natural killer cell receptors involved in MHC class I recognition are disulfide-linked heterodimers of CD94 and NKG2 subunits.

TL;DR: It is demonstrated that CD94 glycoproteins form disulfide-bonded heterodimers with the NKG2A/B, NKG 2C, andNKG2E gly Coproteins, providing for the creation of a diverse NK cell repertoire.
Journal ArticleDOI

DLL4 blockade inhibits tumor growth and reduces tumor-initiating cell frequency.

TL;DR: It is found that specifically inhibiting human DLL4 in the tumor, either alone or in combination with the chemotherapeutic agent irinotecan, reduced cancer stem cell frequency, as shown by flow cytometric and in vivo tumorigenicity studies.