Journal of Clinical & Experimental OncologyISSN: 2324-9110

All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Commentary,  J Clin Exp Onco Vol: 12 Issue: 2

Analysing the Complexities of Pancreatic Cancer and its Mechanism

Jeong Freek*

Department of Pancreatic Surgery, Huazhong University of Science and Technology, Wuhan, China

*Corresponding Author: Jeong Freek
Department of Pancreatic Surgery, Huazhong University of Science and Technology Wuhan, China
E-mail: jeong_freek@hust.cn

Received date: 22 March, 2023, Manuscript No. JCEOG-23-99324;
Editor assigned date: 24 March, 2023, PreQC No. JCEOG-23-99324 (PQ);
Reviewed date: 07 April, 2023, QC No. JCEOG-23-99324;
Revised date: 14 April, 2023, Manuscript No. JCEOG-23-99324 (R);
Published date: 21 April, 2023, DOI: 10.4172/2324-9110.1000346.

Citation: Freek J (2023) Analysing the Complexities of Pancreatic Cancer and its Mechanism. J Clin Exp Oncol 12:2.

Description

Pancreatic cancer is one of the most challenging and enigmatic malignancies, known for its invasive nature and poor prognosis. Pancreatic cancer arises from the uncontrolled growth of cells in the tissues of the pancreas, a vital organ responsible for producing enzymes and hormones involved in digestion and blood sugar regulation. By understanding the complex interplay of factors involved in pancreatic cancer development and progression, one can pave the way for improved diagnostic techniques, treatment strategies, and potential avenues for prevention. Several key mechanisms contribute to the development and progression of pancreatic cancer. Genetic mutations, particularly in tumour suppressor genes such as Tumor protein (TP53) and Cyclin Dependent Kinase Inhibitor 2A (CDKN2A) and oncogenes such as Kirsten Rat Sarcoma Viral Oncogene (KRAS), play a significant role in pancreatic cancer. Mutations in these genes disrupt cell growth regulation and promote uncontrolled proliferation. The pancreatic tumour microenvironment is characterized by an inflammatory response, a desmoplastic reaction, and the presence of stromal cells. These components develop a complex network that supports tumour growth, angiogenesis, immune evasion, and resistance to therapy.

Dysregulation of key signaling pathways, such as the Epidermal Growth Factor Receptor (EGFR), Phospho-Inositide 3 Kinase (PI3K), and Wingless-related Integration site (WNT pathways), contributes to the development and progression of pancreatic cancer. Activation of these pathways promotes cell survival, proliferation, invasion, and metastasis. Pancreatic cancer exerts a profound impact on individuals' health and well-being, both physically and emotionally. The effects vary depending on the stage of the disease and its spread to surrounding tissues or distant organs. Pancreatic cancer can impair the normal function of the pancreas, leading to digestive complications. Individuals may experience difficulties in digesting food, resulting in weight loss, malnutrition, and weakness. Tumours located in the head of the pancreas can obstruct the bile ducts, causing jaundice, yellowing of the skin and eyes, dark urine, and pale stools. This can lead to itching, abdominal pain, and an increased risk of infection.

Pancreatic cancer often presents with severe abdominal pain. The tumour can invade surrounding nerves and organs, leading to persistent pain that may require comprehensive pain management strategies for relief. Unintentional weight loss and fatigue are common in pancreatic cancer. The metabolic demands of the tumour, coupled with decreased appetite and the body's response to cancer, contribute to weight loss and a generalized feeling of tiredness. The complex nature of pancreatic cancer poses significant challenges for healthcare systems, clinicians, and experts. Early detection remains a formidable task due to the lack of specific symptoms and effective screening methods. Additionally, the invasive behaviour of pancreatic cancer and its resistance to conventional therapies limit treatment options and contribute to the low survival rates associated with this disease.

To address these challenges, continued studies are needed to unravel the underlying mechanisms of pancreatic cancer and identify new therapeutic targets advances in precision medicine and immunotherapy provide potential for personalised treatment approaches that may improve outcomes for pancreatic cancer patients. Additionally, raising awareness about the risk factors and symptoms of pancreatic cancer can facilitate early diagnosis and prompt intervention.

Conclusion

Pancreatic cancer continues to present a formidable challenge in the field of oncology. By understanding the intricate mechanisms driving its development, the devastating effects it has on individuals, and the broader implications for healthcare, one can strive towards improved strategies for prevention, diagnosis, and treatment. Efforts to unravel the enigma of pancreatic cancer require multidisciplinary collaboration, innovative studies, and enhanced public awareness. With continued studies and advancements, one can able to transform the landscape of pancreatic cancer and improve the lives of those affected by this complex disease.

international publisher, scitechnol, subscription journals, subscription, international, publisher, science

Track Your Manuscript

Awards Nomination

Media Partners