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Culture and Imaging of Ex Vivo Organotypic Pseudomyxoma Peritonei Tumor Slices from Resected Human Tumor Specimens
Published on: December 9, 2022
Secreted mucins in pseudomyxoma peritonei: pathophysiological significance and potential therapeutic prospects
Afshin Amini, Samar Masoumi-Moghaddam, Anahid Ehteda
1Department of Surgery, St George Hospital, The University of New South Wales, Level 3, Clinical Sciences (WR Pitney) Building, Gray Street, Kogarah, Sydney, NSW 2217, Australia. david.morris@unsw.edu.au.
Abstract:
Pseudomyxoma peritonei (PMP, ORPHA26790) is a clinical syndrome characterized by progressive dissemination of mucinous tumors and mucinous ascites in the abdomen and pelvis. PMP is a rare disease with an estimated incidence of 1-2 out of a million. Clinically, PMP usually presents with a variety of unspecific signs and symptoms, including abdominal pain and distention, ascites or even bowel obstruction. It is also diagnosed incidentally at surgical or non-surgical investigations of the abdominopelvic viscera. PMP is a neoplastic disease originating from a primary mucinous tumor of the appendix with a distinctive pattern of the peritoneal spread. Computed tomography and histopathology are the most reliable diagnostic modalities. The differential diagnosis of the disease includes secondary peritoneal carcinomatoses and some rare peritoneal conditions. Optimal elimination of mucin and the mucin-secreting tumor comprises the current standard of care for PMP offered in specialized centers as visceral resections and peritonectomy combined with intraperitoneal chemotherapy. This multidisciplinary approach has reportedly provided a median survival rate of 16.3 years, a median progression-free survival rate of 8.2 years and 10- and 15-year survival rates of 63% and 59%, respectively. Despite its indolent, bland nature as a neoplasm, PMP is a debilitating condition that severely impacts quality of life. It tends to be diagnosed at advanced stages and frequently recurs after treatment. Being ignored in research, however, PMP remains a challenging, enigmatic entity. Clinicopathological features of the PMP syndrome and its morbid complications closely correspond with the multifocal distribution of the secreted mucin collections and mucin-secreting implants. Novel strategies are thus required to facilitate macroscopic, as well as microscopic, elimination of mucin and its source as the key components of the disease. In this regard, MUC2, MUC5AC and MUC5B have been found as the secreted mucins of relevance in PMP. Development of mucin-targeted therapies could be a promising avenue for future research which is addressed in this article.
Insights
Pseudomyxoma peritonei (PMP) is a rare abdominal cancer causing mucinous tumors and ascites. Novel mucin-targeted therapies are needed for this challenging disease.
Area of Science:
- Oncology
- Gastroenterology
- Rare Diseases
Background:
- Pseudomyxoma peritonei (PMP) is a rare neoplastic syndrome characterized by mucinous tumor dissemination and ascites.
- It originates from appendiceal mucinous tumors and presents with non-specific symptoms, often diagnosed incidentally.
- PMP significantly impacts quality of life and frequently recurs despite treatment.
Purpose of the Study:
- To review the clinicopathological features of PMP.
- To discuss current treatment standards and outcomes.
- To highlight the need for novel therapeutic strategies targeting mucin in PMP.
Main Methods:
- Review of existing literature on PMP.
- Analysis of diagnostic modalities including computed tomography and histopathology.
- Evaluation of current treatment approaches: cytoreductive surgery and hyperthermic intraperitoneal chemotherapy.
Main Results:
- The multidisciplinary approach offers a median survival of 16.3 years, with 10- and 15-year survival rates of 63% and 59%.
- PMP is characterized by mucin secretion and peritoneal spread, with MUC2, MUC5AC, and MUC5B identified as relevant mucins.
- Despite indolent behavior, PMP is debilitating, diagnosed late, and prone to recurrence.
Conclusions:
- Current treatments improve survival but novel strategies are essential for complete elimination of mucin and tumors.
- Targeting specific secreted mucins (MUC2, MUC5AC, MUC5B) represents a promising future research direction.
- Further research into mucin-targeted therapies is crucial for advancing PMP management.
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