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Enrichment and Characterization of the Tumor Immune and Non-immune Microenvironments in Established Subcutaneous Murine Tumors
Published on: June 7, 2018
Tumor Microenvironment Proteomics: Lessons From Multiple Myeloma
Rodrigo Carlini Fernando1, Fabrício de Carvalho1, Adriana Franco Paes Leme2
1Department of Experimental and Clinical Oncology, Discipline of Hematology and Hemotherapy, Federal University of São Paulo, UNIFESP, São Paulo, Brazil.
Abstract:
Although the "seed and soil" hypothesis was proposed by Stephen Paget at the end of the 19th century, where he postulated that tumor cells (seeds) need a propitious medium (soil) to be able to establish metastases, only recently the tumor microenvironment started to be more studied in the field of Oncology. Multiple myeloma (MM), a malignancy of plasma cells, can be considered one of the types of cancers where there is more evidence in the literature of the central role that the bone marrow (BM) microenvironment plays, contributing to proliferation, survival, migration, and drug resistance of tumor cells. Despite all advances in the therapeutic arsenal for MM treatment in the last years, the disease remains incurable. Thus, studies aiming a better understanding of the pathophysiology of the disease, as well as searching for new therapeutic targets are necessary and welcome. Therefore, the present study aimed to evaluate the protein expression profiling of mononuclear cells derived from BM of MM patients in comparison with these same cell types derived from healthy individuals, in order to fill this gap in MM treatment. Proteomic analysis was performed using the mass spectrometry technique and further analyses were done using bioinformatics tools, to identify dysregulated biological pathways and/or processes in the BM microenvironment of patients with MM as a result of the disease. Among the pathways identified in this study, we can highlight an upregulation of proteins related to protein biosynthesis, especially chaperone proteins, in patients with MM. Additionally, we also found an upregulation of several proteins involved in energy metabolism, which is one of the cancer hallmarks. Finally, with regard to the downregulated proteins, we can highlight mainly those involved in different pathways of the immune response, corroborating the data that has demonstrated that the immune system of MM is impaired and, therefore, the immunotherapies that have been studied recently for the treatment of the disease are extremely necessary in the search for a control and a cure for these patients who live with the disease.
Insights
This study compared bone marrow cells from multiple myeloma (MM) patients and healthy individuals. MM patients showed increased protein biosynthesis and energy metabolism, alongside impaired immune responses, highlighting new therapeutic targets for this incurable cancer.
Area of Science:
- Oncology
- Proteomics
- Cancer Biology
Background:
- The "seed and soil" hypothesis highlights the tumor microenvironment's role in metastasis.
- Multiple myeloma (MM) bone marrow microenvironment is crucial for cancer cell survival and drug resistance.
- Despite therapeutic advances, MM remains incurable, necessitating further research into its pathophysiology.
Purpose of the Study:
- To investigate protein expression profiling in bone marrow mononuclear cells from MM patients versus healthy individuals.
- To identify dysregulated biological pathways and processes in the MM bone marrow microenvironment.
- To uncover potential new therapeutic targets for MM treatment.
Main Methods:
- Proteomic analysis using mass spectrometry.
- Bioinformatic tools for pathway and process analysis.
- Comparison of protein expression between MM patients and healthy controls.
Main Results:
- Upregulation of proteins involved in protein biosynthesis, particularly chaperone proteins, in MM patients.
- Increased expression of proteins related to energy metabolism, a hallmark of cancer.
- Downregulation of proteins associated with immune response pathways, indicating immune impairment in MM.
Conclusions:
- The bone marrow microenvironment in MM exhibits altered protein expression, including enhanced protein synthesis and energy metabolism.
- Impaired immune responses in MM patients underscore the need for immunotherapies.
- These findings provide insights into MM pathophysiology and suggest potential therapeutic strategies.
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