Skip to main content
Biological pathway icon

Biological Pathway Reviews

Mutation Type Summary Cancer Type View

AKT (protein kinase B) is a serine threonine kinase that plays a pivotal role in regulating many cell processes, including survival, proliferation, invasion, apoptosis, and angiogenesis.1 Disruptions in the AKT pathway are associated with cancer, diabetes, cardiovascular and neurological diseases.2 In breast cancer, AKT is disrupted in up to 70% of cases, making it a valua

Breast Cancer View
GPRC5D

G protein-coupled receptor class C group 5 member D (GPRC5D) is a gene expressed in the hair follicle and malignant bone marrow plasma cells.1 G protein-coupled receptor proteins are cell surface receptors located in the plasma membrane.

Multiple Myeloma View
HER2

Human epidermal growth factor receptor 2 (HER2) is 1 of 4 transmembrane tyrosine kinase receptor proteins in the epidermal growth factor receptor family.1,2 Normally expressed on epithelial cellular membranes of organs such as breast and skin, HER2 exists in other tissues, includi

Bladder Cancer; Breast Cancer; Cervical Cancer; Cholangiocarcinoma; Colorectal Cancer; Endometrial Cancer; Esophageal Cancer; Gallbladder Cancer; Gastric Cancer; Head and Neck Cancer; Lung Cancer; Ovarian Cancer; Pancreatic Cancer; Prostate Cancer; Salivary Cancer; Testicular Cancer; Uterine Cancer; Vaginal Cancer View
HRR

Homologous recombination repair (HHR) is a DNA repair mechanism that removes damaged DNA by acting on double-strand breaks, interstrand crosslinks, and other kinds of DNA damage.1 DNA damage is repaired with high fidelity by correcting damage with information copied from a homologous undamaged molecule.2 Defects in HRR are present in some cancers.3

View
20S Proteasome

The ubiquitin-proteasome system (UPS) is the essential system within the body to ensure elimination of misfolded proteins.1 Proteins which are to be degraded are tagged with polyubiquitin chains, which are recognized by 19S.1 This particle, 19S, along with the 20S proteasome core, form the 26S proteasome overall.1 One protein the 20S proteasome targe

Mantle Cell Lymphoma; Multiple Myeloma View
ALK

ALK is a tyrosine kinase receptor that resides on chromosome 2p23. Chromosomal rearrangements resulting in fusion genes leads to ALK tyrosine kinase that promote cell survival by activating a signaling pathway or by inhibition of apoptosis, which leads to cell proliferation.1

ALCL; Breast Cancer; Colorectal Cancer; DLBCL; Inflammatory Myofibroblastic Tumors; Neuroblastoma; NSCLC View
BCL2

Tumor cells have many characteristics, including genomic instability and oncogene activation, which should lead to apoptosis.1 In a bid to survive, tumor cells may become dependent on the BCL-2 protein.2 Certain cancer cells will overexpress BCL-2, which in turn impedes apoptosis and facilitates tumor growth and resistance to chemotherapy.3 These mal

ALL; AML; CLL; DLBCL; Follicular Lymphoma; Head and Neck Cancer; Lung Cancer; NSCLC; Prostate Cancer; Solid Tumors View
BCMA

BCMA is a member of the tumor necrosis factor receptor family that is expressed on plasma cells and on late stage normal and malignant B-cells.1 BCMA binds to BAFF, activating the NF-kB and MAPK8/JNK signaling pathways, which leads to the prolif

AML; CLL; DLBCL; Follicular Lymphoma; Hodgkin Lymphoma; Multiple Myeloma; T-cell Lymphoma View
BRAF

Oncogenic mutations in BRAF genes activate the RAF/MEK/ERK pathway, resulting in increased cell proliferation and resistance to apoptosis.1 BRAF mutations have been identified in 7% to 8% of all cancers.2 V600E is the most common activating mutations in BRAF and is associated with more

Colorectal Cancer; Hairy Cell Leukemia; Lung Cancer; Melanoma; Multiple Myeloma; Thyroid Cancer View