New Database Aims to Aid Pancreatic Cancer Research
A user-friendly tool to connect datasets and improve research on pancreatic cancer.
Claude Chelala, J. Oscanoa, H. Ross-Adams, A. Z. M. Dayem Ullah, T. S. Kolvekar, L. Sivapalan, E. Gadaleta, G. J. Thorn, M. Abdollahyan, A. Imrali, A. Saad, R. Roberts, C. Hughes, PCRFTB, H. M. Kocher
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Table of Contents
Pancreatic ductal adenocarcinoma (PDAC) is a type of cancer that starts in the pancreas. It is expected to become the second leading cause of cancer deaths worldwide soon. Unfortunately, PDAC has very low survival rates, with only about 3-15% of patients living for five years after diagnosis. This is mainly because the disease is often detected late and there are not many effective treatment options available. The situation is getting worse, as more younger people are being diagnosed with pancreatic cancer compared to other solid tumors. Therefore, better tools to classify patients and track how well treatments work are very important for improving survival rates.
However, the field of pancreatic cancer research is small. Researchers often create their own unique collections of samples, but these may not be useful outside of the specific conditions they are stored in. Different methods of collecting samples also make it hard to apply findings for the benefit of patients.
Most current markers used to monitor treatment or predict outcomes are not based on the actual details of PDAC tumors. These markers have been shown to have limited effectiveness in real-world situations. While many studies have looked into the genetic and Molecular aspects of tumor growth, the results are scattered across various resources and can be hard to access for those without advanced computer skills. This shows a clear need for simpler tools that help researchers analyze and visualize data from different sources so they can better understand pancreatic diseases.
Introducing the Pancreatic Expression Database (PED)
To address these issues, a new online tool called the Pancreatic Expression Database (PED) has been set up. This user-friendly portal connects various datasets to a Biobank where researchers can validate their findings and request samples for further study. PED has undergone important updates to its analysis features and now includes a wider range of datasets. It also works together with the UK's national Pancreatic Cancer Research Fund Tissue Bank (PCRFTB) to facilitate research and data sharing between doctors and scientists.
The PCRFTB is the first national tissue bank dedicated to the pancreas and has been collecting samples from patients at several hospitals since 2015. This biobank includes blood, urine, saliva, tissue samples, cancer organoids, and other biological materials related to pancreatic and liver diseases, including both operable and inoperable cancers. Along with these samples, there is extensive clinical, imaging, and other data available for researchers. The quality of these biological materials is ensured through standard practices, allowing for reliable research outcomes.
How PED Works
Through PED, researchers can search for and apply to obtain samples and information that fit their research needs. A direct link to the PCRFTB Tissue Request System makes it easy for users to submit applications.
The main goal of the PED is to provide a centralized hub for analyzing publicly available pancreatic datasets alongside ongoing research data. This will give researchers fast and free access to a wide range of important information. The flexibility of this hub allows for identifying and prioritizing critical genetic changes that could be explored further.
Updates to the Analytics Hub
The web-based Analytics Hub has been updated to include many publicly available datasets related to pancreatic cancer, along with new analysis and visualization tools based on feedback from users around the world.
This updated analytics hub includes clinical and molecular datasets from several key sources. Researchers can filter the data based on various factors related to the patients and their tumors. This makes it easier to look for trends and useful information, such as survival rates in different types of pancreatic cancer.
Understanding Molecular Subtypes
With PED, researchers can also analyze tumor samples based on their molecular characteristics. This classification can help identify different types of PDAC tumors, which may respond differently to treatments. For example, some classifications use RNA sequencing, which looks at how genes are expressed in tumors.
Research has shown that PDAC tumors can be divided into different subtypes, each of which has unique features and outcomes. These classifications have been linked to how patients respond to treatments. For instance, some subtypes are associated with better survival, while others indicate a worse prognosis.
Key Findings
The analysis of various PDAC tumor subtypes has revealed important genetic changes. Different subtypes exhibit different patterns of gene mutations, which can influence treatment effectiveness. For example, certain mutations in genes like KRAS and TP53 appear in many tumors but show variation between subtypes.
Recent studies have been able to identify promising treatment options based on these unique genetic patterns. For instance, patients with specific KRAS mutations may benefit from targeted therapies that aim to block the activity of mutant proteins.
The Importance of Quality Samples
Access to high-quality samples is crucial for understanding pancreatic cancer and identifying new treatments. The PCRFTB is dedicated to collecting and managing these samples effectively, allowing researchers to conduct meaningful studies.
There is also an effort to return data from studies that use these samples to the biobank, ensuring that valuable information is available for future research. This policy encourages collaboration and sharing of knowledge within the pancreatic cancer research community.
Looking Ahead
As research continues to advance, tools like the PED will play a key role in improving our understanding of pancreatic cancer. By providing access to valuable datasets and samples, researchers can uncover new insights that may lead to better diagnosis, treatment, and ultimately improved outcomes for patients.
PED fosters a collaborative environment where data can be easily shared and analyzed, opening the door for innovative research and potentially life-saving discoveries. As the field of pancreatic cancer research expands, the integration of clinical and molecular data will help researchers refine their approaches to treatment and improve patient care.
With ongoing updates and improvements, PED is paving the way for future breakthroughs in the fight against pancreatic cancer. The availability of diverse datasets, coupled with robust analysis tools, allows researchers to explore the complexities of this disease and push the boundaries of science in search of effective treatments.
In conclusion, the challenges presented by pancreatic cancer are significant, but with resources like the Pancreatic Expression Database and the support of initiatives like the PCRFTB, there is hope for more effective research and treatment strategies moving forward. By focusing on collaboration and sharing of knowledge, the pancreatic cancer research community is taking important steps toward overcoming the obstacles faced in this complex and often devastating disease.
Original Source
Title: A central research portal for mining pancreatic clinical and molecular datasets and accessing biobanked samples
Abstract: The Pancreas Genome Phenome Atlas (PGPA) is dedicated to the analysis of pancreatic datasets from four primary sources (Cancer Genome Atlas, International Cancer Genome Consortium, Cancer Cell Line Encyclopaedia, Genomics Evidence Neoplasia Information Exchange) that together form the foundation of -omics profiling of pancreatic malignancies and related lesions (n=7,760 specimens). Multiple user-friendly analytical tools to explore the associated molecular data from these primary specimens and cell lines are available. Crucially, PGPA is the access point for Pancreatic Cancer Research Fund Tissue Bank - the only national pancreatic cancer biobank in the UK, and will facilitate effective sharing of multi-modal molecular, histopathology and imaging data from biobank samples (>60,000 specimens from >3,400 cases and controls; 2,037 H&E images from 349 donors) and accelerate validation of in silico findings in patient-derived material. This places PGPA at the forefront of biomarker-based research, providing the user community with a distinct resource to facilitate hypothesis-testing on public data, validate novel research findings, and access curated, high-quality patient tissues for translational research. To demonstrate the practical utility of PGPA, we investigate somatic variants associated with established transcriptomic subtypes and disease prognosis: several patient-specific variants are clinically actionable and may be leveraged for precision medicine.
Authors: Claude Chelala, J. Oscanoa, H. Ross-Adams, A. Z. M. Dayem Ullah, T. S. Kolvekar, L. Sivapalan, E. Gadaleta, G. J. Thorn, M. Abdollahyan, A. Imrali, A. Saad, R. Roberts, C. Hughes, PCRFTB, H. M. Kocher
Last Update: 2024-12-17 00:00:00
Language: English
Source URL: https://www.medrxiv.org/content/10.1101/2024.07.25.24309825
Source PDF: https://www.medrxiv.org/content/10.1101/2024.07.25.24309825.full.pdf
Licence: https://creativecommons.org/licenses/by/4.0/
Changes: This summary was created with assistance from AI and may have inaccuracies. For accurate information, please refer to the original source documents linked here.
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