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Cancer stem cells (CSCs) are a subpopulation of cells within tumors that possess the ability to self-renew and drive tumor growth and metastasis. These cells are thought to be responsible for cancer recurrence and resistance to conventional therapies, as they can evade treatments that target rapidly dividing cells. Understanding the biology of CSCs is crucial for developing more effective, targeted therapies aimed at eradicating these cells and improving patient outcomes in cancer treatment.

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Colorectal cancer starts in the colon or the rectum. It’s named by colon cancer or rectal cancer, where they start depending in colon cancer and rectal cancer are repeatedly grouped together because they have many features in common. When cells in the body cancer will start to grow out of control. It nearly any part of the body can become cancer and can spread to other areas of the body.

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Skin Cancer is the abnormal growth of cells in the outer most layer of the skin caused by unpaired DNA damage, that trigger mutations, which appear like a lump or discolor the patch of the skin. The mutation leads the skin cells to multiply rapidly and form tumors. The common skin cancers are Basal Cell Carcinoma, Squamous Cell Carcinoma, Merkel Cell Carcinoma, and Melanoma. Skin cancer develops in the area of the body that is regularly exposed to ultraviolet (UV) rays from the sun such as the nose, neck, arms, legs, lips, chest, scalp, face etc.

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It is the type of organ related cancer which mainly occurs in tissues of the breast. The most common types of breast cancers are Ductal Carcinoma Insitu (DCIS) and Invasive Carcinoma. Inflammatory Breast Cancer and Metastatic Breast Cancer, Triple-Negative Breast Cancer. Among these Triple-Negative Breast Cancer (TNBC) is the worst breast cancer. Breast cancer mainly starts in the gland cells in the lobules. Breast cancer is one of the most common cancers in females than in males. It can occur at any age but in adults mostly it occurs over the age of 50.

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Cancer is a hereditary disease. Changes in genes that control how cells grow and multiply cause it. Cells are the fundamental building blocks of your body. Each cell has a duplicate of your genes, which serves as an instruction manual. Cancer is a genetic disease in which tumor cells differ from their normal progenitors due to genetic changes affecting growth-regulatory genes. There are two types of cancer genes: oncogenes (which act as positive growth regulators) and tumor suppressor genes (which act as negative growth regulators).

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Head and Neck cancer is a type of cancer which is used to describe the various malignant tumors that occur in or around the head and neck parts such as Nose, Larynx, Mouth, Throat, Sinus. Types of head and neck cancers are Nasal cavity, Paranasal sinus Cancer, Oral and Pharyngeal Cancer, Salivary Gland Cancer, Laryngeal and Hypo Pharyngeal Cancer, Thyroid cancer, Eye cancer, Brain Tumor, Esophageal Cancer, Sarcoma, Parathyroid Cancer. The most common cause of Head and Neck Cancer are due to tobacco and alcohol use.

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Most blood cancers, also known as hematologic cancers, begin in the bone marrow, where blood is produced. Blood cancers develop when abnormal blood cells begin to proliferate uncontrollably, interfering with the function of normal blood cells, which fight infection and produce new blood cells. There are three main types of blood cancers: leukemia, lymphoma, and myeloma. Leukemia is a cancer of the blood and bone marrow that affects white blood cells. Lymphoma is a cancer that begins in the lymphatic system, which is part of the immune system. Myeloma is a cancer that affects plasma cells, which are a type of white blood cell that produces antibodies. Symptoms of blood cancer can include fatigue, weakness, fever, weight loss, and enlarged lymph nodes.

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Genitourinary cancer refers to cancers affecting the urinary system and the male and female reproductive organs. This includes common types such as prostate, bladder, kidney, and testicular cancers in men, and cervical, ovarian, and urethral cancers in women. Risk factors vary by cancer type but may include genetics, environmental exposures, and lifestyle choices. Early detection and advances in treatment options, such as surgery, radiation therapy, and immunotherapy, are crucial for improving patient outcomes in genitourinary cancers.

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Childhood cancer refers to cancers that occur in children, typically affecting individuals aged 0 to 19 years. The most common types include leukemia, brain tumors, and neuroblastoma. While childhood cancers are rare compared to adult cancers, they often require specialized treatment approaches and can significantly impact a child’s development and quality of life. Advances in treatment, including chemotherapy, radiation, and targeted therapies, have improved survival rates, but ongoing research is essential to enhance outcomes and address long-term effects.

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It is a type of cancer which occurs in bone or in the soft tissues in the body, including cartilage, fat, muscle, blood vessels, and fibrous tissues. The most common types of sarcomas are Osteosarcoma, Fibrosarcoma, Chondrosarcoma, Dermatofibrosarcoma, Pleomorphic sarcoma. Pleomorphic sarcoma is the rarest, but it is a very dangerous sarcoma caused due to the exposure of harmful chemicals and radiation.

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Certain infections can lead to cancer by causing chronic inflammation, immune suppression, or directly altering cell genetics. Viruses like HPV and Hepatitis B and C are linked to cervical and liver cancers, respectively, while Epstein-Barr virus (EBV) and HIV increase the risk of lymphomas. Helicobacter pylori bacteria can contribute to gastric cancer, and parasites like Schistosoma haematobium are associated with bladder cancer. Vaccinations, treating infections, and regular screenings are essential strategies to help prevent cancers caused by these infectious agents.

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Cancer genetics and epigenetics study how genetic mutations and epigenetic modifications drive cancer. Genetic changes, like mutations in oncogenes and tumor suppressor genes, alter cell behavior, leading to uncontrolled growth. Epigenetic modifications, such as DNA methylation and histone changes, affect gene expression without altering DNA sequences, potentially silencing tumor-suppressing genes or activating oncogenes. Together, these insights help identify biomarkers for early detection and personalized treatments, with therapies now targeting both genetic mutations and epigenetic changes to improve cancer outcomes.

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Thoracic oncology focuses on the diagnosis and treatment of cancers in the chest region, primarily lung cancer, but also includes tumors of the pleura, mediastinum, and chest wall. Lung cancer is the leading cause of cancer-related deaths worldwide and is often categorized into non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC). Risk factors include smoking, environmental exposures, and genetic predispositions. Advances in imaging, targeted therapies, and immunotherapy are enhancing early detection and treatment outcomes in thoracic oncology.

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Molecular cancer biology explores the cellular and molecular mechanisms that drive cancer, focusing on how genetic mutations, signaling pathways, and interactions within the tumor microenvironment contribute to cancer growth and spread. It examines the role of oncogenes, tumor suppressor genes, and regulatory pathways, such as those involving cell cycle control and apoptosis, in tumor initiation and progression. By understanding these molecular processes, researchers aim to develop targeted therapies that disrupt cancer-specific pathways, leading to more effective and personalized cancer treatments.

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