Oesophageal cancer (EC) is an aggressive malignancy with high incidence and mortality rates. It is the sixth major cause of cancer-related deaths worldwide, with the developing countries bearing nearly 80% of the total burden of this cancer. Despite advancements in multimodality therapy, the prognosis for patients with EC remains poor. One of the significant hurdles in the effective management of EC is the development of chemoresistance in patients during treatment. Advances in experimental tools facilitate a better understanding of the mechanism underlying cancer development and thus aid in designing effective diagnostic and therapeutic strategies. In this regard, in vitro assays, and in vivo animal models are essential tools in cancer research that enable researchers to develop novel cancer therapies, drug screening methods, and provide insight into the molecular mechanisms of tumor growth and metastasis.
Recent advances in developing three-dimensional (3D) cell cultures, such as transwell-based, spheroid-based, tumor-microvessel models, and patient-derived organoids, have revolutionized cancer investigation. These 3D cultures have emerged as more efficient model systems than the 2D cell line platform. They better mimic the tumor complexity through possible coculturing, incorporation of biomaterials, microfabrication, and microfluidics. There is also an increasing interest in using omics technologies to characterize molecular changes underlying the development of this deadly disease and identify biomarkers for early diagnosis, prognosis, and predicting response to therapy.
This Methods Collection aims to be a visual resource of (in-vitro, in-vivo, and clinical) protocols used in oesophageal cancer research, from unraveling underlying molecular mechanisms to developing biomarkers and therapeutic targets to drug screening and treatment.
0 Views
•
Cited by 10
•
2022
•
Samuel Flashner*1, Cecilia Martin*1,2, Norihiro Matsuura1, Masataka Shimonosono1, Yasuto Tomita1, Masaki Morimoto1, Ogoegbunam Okolo1, Victoria X. Yu1,3, Anuraag S. Parikh1,3, Andres J. P. Klein-Szanto4, Kelley Yan1,2, Joel T. Gabre1,5, Chao Lu1,6, Fatemeh Momen-Heravi1,7, Anil K. Rustgi1,5, Hiroshi Nakagawa1,2,5
1Herbert Irving Comprehensive Cancer Center, Columbia University, 2Organoid and Cell Culture Core, Columbia University Digestive and Liver Diseases Research Center, Columbia University, 3Department of Otolaryngology, Head and Neck Surgery, Columbia University, 4Histopathology Facility, Fox Chase Cancer Center, 5Division of Digestive and Liver Diseases, Department of Medicine, Columbia University, 6Department of Genetics and Development, Columbia University, 7Section of Oral, Diagnostic and Rehabilitation Sciences, College of Dental Medicine, Columbia University
0 Views
•
Cited by 3
•
2024
•