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January 1, 2017

PC-3M-Luc-C6 – a model for prostate carcinoma

Early detection of prostate cancer is very challenging. Unfortunately patients are asymptomatic until advanced stage disease, leaving them with limited treatment options. The delayed detection also results in an increase in the incidence of metastatic disease. Advanced stage prostate cancer typically metastasizes to the bone and lymph nodes.
February 1, 2017

GL261-luc: A model for immunotherapy and radiation therapy

Glioblastoma multiforme (GBM) is the most aggressive form of brain cancer. GBM tumors grow within a fairly immunosuppressive tumor microenvironment and a relatively immune-privileged central nervous system. For patients diagnosed with GBM, prognosis remains poor with conventional therapies that include radiotherapy, chemotherapy, and surgery.
October 1, 2019

LL/2: an immunosuppressive murine tumor model

Lung cancer is the second most common cancer diagnosed in both men and women in the United States and is, by far, the most common cause of cancer-related deaths in men and women. In 2019, the American Cancer Society estimates that 228,150 new cases of lung cancer (116,440 in men and 111,710 in women) will be diagnosed, and 142,670 deaths from lung cancer (76,650 in men and 66,020 in women) will occur.
March 1, 2018

Models for non-small cell lung carcinoma - part 2

As we presented in last month’s model spotlight, lung cancer is a devastating disease and is the leading cause of cancer death in the US and worldwide.1 The research community continues to look for new models that will aid in lung cancer research. The ATCC (a widely used cell repository) currently has over 100 different human derived lung cancer cell lines.
January 1, 2016

GL261: Syngeneic murine glioma model

Glioblastomas are known to have a poor prognosis with median survival of nine months and only five to 10 percent of patients surviving up to two years. Conventional therapies include radiotherapies and surgical removal of the tumor in combination with chemotherapy.
January 1, 2019

C1498-Luc-mCherry: A syngeneic acute myeloid leukemia (AML) model

Acute myeloid leukemia (AML) is the most common hematologic malignancy in adults with a 5-year survival rate of ~25% following diagnosis.[1] While two-thirds of AML patients treated with standard high dose chemotherapy achieve remission, 50% of patients relapse after remission. The majority of relapses occur within two to three years of initial treatment, and every patient carries the risk of relapse due to the molecular heterogeneity of the disease.[2] This has created an impetus to explore novel therapeutic approaches; in particular, immune-based therapies, since AML cells express both major histocompatibility complex (MHC) classes I and class II which makes them susceptible targets of innate and adaptive immune responses.[3]
September 1, 2017

Tumor models for pancreatic cancer

More than 90% of all pancreatic cancers are classified as ductal adenocarcinomas and, within the western-world, pancreatic cancer is the fourth leading cause of cancer related deaths. Prognosis with pancreatic cancer is extremely poor, with a 5-year relative survival rate of 5% and median survival of 3.5 months for patients with Stage III non-resectable tumors.1 Unfortunately, the incidence of pancreatic cancer has been on the rise while the 5-year survival rate has not changed. Surgical resection is the only potentially curative therapy, but only 10% of patients are diagnosed early enough for this to be an option and most who are eligible for surgery ultimately relapse. As with many other types of cancer, pancreatic cancer grows silently for years without any symptoms. In most cases diagnosis is not made until the cancer has grown outside of the pancreas to other proximal tissues and/or has metastasized. These patients are left with very few meaningful options. Therefore, effective novel therapies are sorely needed in treatment of pancreatic cancer.