Translational cancer research has taken giant leaps since appearing in the scientific literature at the beginning of the 21st century. It progressed from identifying a single mutation driving cancer to the high-throughput next-generation whole-genome sequencing analyses. Recent advances in omics have broadened our knowledge of the processes underlying cancer development.
In recognition of its importance, we have recently launched a new cross-journal article collection on Translational Oncology, guest edited by Prof Tommaso Dragani. As part of the collection, in a Forum Article, 8 cancer research experts highlight major translational advances in colorectal, ovarian, breast, lung, and prostate cancer research.
The complexity of cancer is ever more apparent with every new discovery. Genome-wide association studies have shown that (…) hundreds of genetic variants conspire to determine that risk [of developing cancer].
Tommaso Dragani in “Major milestones in translational oncology”
Reading their short overviews, it’s clear that we need a tailored approach for each cancer type. The point of convergence is aiming for individualized approaches and precision medicine, in other words designing treatments targeting specific alterations that drive tumor development in individual patients.
BMC Medicine also recently attended the EACR24 Congress in Manchester and UK Breast Cancer Research Symposium 2016 in London (organized by Breast Cancer Now). Many sessions discussed how basic research contributes to informing clinical decisions in oncology.
A key challenge in translational research is tumor heterogeneity. It’s observed at many levels from differences between individuals, differential treatment responses to intratumor heterogeneity. This concept has fuelled studies on cancer mutational signatures, like research from Mike Stratton’s group.
The main aim of such genome-driven studies is establishing tumor clusters that hold “clinically applicable information that could impact treatment decisions”[1]. As summarized by Antoni Castells, a number of molecular classification systems have recently been established for colorectal cancer research.
This new classification approach based on well-differentiated biological profiles may represent a landmark for future clinical stratification and subtype-based targeted interventions. Antoni Castells in “Major milestones in translational oncology”
J.P. Michiel Sedelaar and Jack A. Schalken emphasized the need for molecular stratification of castration-resistant prostate cancer, which may be soon achieved by next generation sequencing studies.
Precision medicine based on the molecular profile of the cancer’s actionable targets can be validated. J.P. Michiel Sedelaar and Jack A. Schalken in “Major milestones in translational oncology”
Recently, the work of the METABRIC Consortium resulted in identifying 10 clusters of breast cancer, as highlighted by Helena Earl. This approach is likely to be enhanced with the use of plasma circulating tumor DNA (ctDNA) as repeatable “liquid biopsies”, which facilitates tracking mutations and treatment response.
In the translational effort, could large clinical trials be replaced by ‘big data’ national and international collections from breast cancer populations? (…) the short answer is ‘yes’. Helena Earl in “Major milestones in translational oncology”
“Liquid biopsies” are important also in lung cancer translational research, as briefly described by Wade T. Iams and Christine M. Lovly. Therapy of lung cancer, beside melanoma, has seen great progress after successful clinical trials of immunotherapeutics.
ctDNA testing has the potential to revolutionize not only how we diagnose and treat lung cancer, but other solid organ tumors as well. Wade T. Iams and Christine M. Lovly in “Major milestones in translational oncology”
The main challenge is acquired treatment resistance both to immune and molecular-targeted therapy. Understanding the role of immune system in cancer development, as discussed during EACR24 Congress by James P. Allison and Adrian Hayday, may help in overcoming tumor escapes.
Targeting resistance mechanisms is a successful paradigm for ongoing research to improve outcomes in lung cancer patients. (…) The combination of different immune checkpoint inhibitors seeks to increase efficacy by addressing more than one pathway through which tumors evade the immune system. Wade T. Iams and Christine M. Lovly in “Major milestones in translational oncology”
Apart from treatment response assessment and risk estimation, molecular profiling is useful in cancer screening. Vathany Kulasingam and Eleftherios P. Diamandis have summarized the key advances in ovarian cancer screening.
[The UKCTOCS study] biorepository [of] longitudinal samples with excellent, linked clinical data that can serve as a useful resource for a broad research community to investigate the prevention, early detection, etiology, and treatment of [ovarian cancer]. Vathany Kulasingam and Eleftherios P. Diamandis in “Major milestones in translational oncology”
Translational research is crucial in informing clinical practice and trials. Bringing researchers and clinicians together, combining clinical information with basic research findings is the way to move the field forward, find the best solutions and beat cancer.
[1] J.P. Michiel Sedelaar and Jack A. Schalken in “Major milestones in translational oncology”
Are you working on novel translational cancer research? Consider submitting your manuscript to our new cross-journal article collection on Translational Oncology. The journals included in this collection are:
- BMC Medicine,
- BMC Cancer,
- Cancers of the Head and Neck,
- Clinical Sarcoma Research and
- Journal of Experimental and Clinical Cancer Research.
The article collection is now accepting submissions of original research articles that provide important developments in cancer research. Preclinical studies should provide a significant advance in knowledge, and have clear potential for strong clinical impact.
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