Transforming Insights Into Innovation
At Dimer Pharmaceuticals, we are committed to tackling the most aggressive and life-threatening cancers by targeting critical drivers of disease progression. One such driver is MYCN amplification, a genetic alteration that underpins tumor growth, resistance, and metastasis in several cancer types. With our unique approach inspired by prion biology and protein homeostasis, we aim to disrupt the devastating impact of MYCN amplification and offer hope to patients.
What is MYCN Amplification?
MYCN amplification is characterized by an increase in the number of copies of the MYCN gene, leading to its overexpression. This amplification drives a cascade of molecular events that fuel rapid tumor growth, evade immune defenses, and resist conventional therapies. MYCN is particularly challenging because of its role as a master regulator of cellular processes, including:
Cell Cycle Regulation
Metabolic Reprogramming
Survival Pathways
Tumor Microenvironment Modulation
Cancers Driven by MYCN Amplification
MYCN amplification is a hallmark of various cancers, driving aggressive tumor growth, metastasis, and therapy resistance. These cancers are part of Dimer Pharmaceuticals' Platform Technology to address all MYC-N Driven Cancers.
Neuroblastoma
A common pediatric cancer arising in the adrenal glands or sympathetic nervous system. High-risk cases often resist therapy and have poor survival rates.
Medulloblastoma
A malignant brain tumor in children, originating in the cerebellum, with aggressive subtypes prone to rapid spread and long-term neurocognitive impacts.Diffuse Intrinsic Pontine Glioma (DIPG)
A fatal pediatric brainstem tumor affecting critical functions, with no effective treatments and a median survival of less than a year.Embryonal Tumor with Multilayered Rosettes (ETMR)
A rare and fast-growing brain tumor in children, resistant to therapy and associated with poor outcomes.Atypical Teratoid/Rhabdoid Tumors (AT/RT)
Highly malignant brain tumors in young children with low survival rates, despite aggressive therapy.Pineoblastoma
A rare tumor of the pineal gland causing headaches and hydrocephalus, with limited treatment success due to its location.Supratentorial Primitive Neuroectodermal Tumors (sPNETs)
Rare and aggressive brain tumors in children, often resistant to therapy with poor prognosis.Ependymomas
Tumors of the brain or spinal cord lining, common in children, with frequent recurrence in higher-grade cases.Rhabdomyosarcoma
A childhood soft tissue cancer, with the alveolar subtype being aggressive and prone to metastasis.Glioblastoma (GBM)
An aggressive adult brain tumor known for rapid growth, resistance to treatment, and a median survival of just 15 months.Small Cell Lung Cancer (SCLC)
A fast-growing, smoking-associated lung cancer with poor survival rates, often diagnosed at an advanced stage.Neuroendocrine Prostate Cancer
A highly aggressive prostate cancer subtype, often developing resistance to hormonal therapies.Prostate Adenocarcinoma
A common prostate cancer type that is more challenging to treat in advanced or metastatic stages.Wilms’ Tumor
A kidney cancer in children under five, often treatable but more aggressive in high-risk cases.Retinoblastoma
A pediatric eye cancer detected by a white reflection in the pupil, with good outcomes if caught early.Basal Cell Carcinoma
The most common skin cancer, usually slow-growing but occasionally aggressive in rare cases.