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5HIAA as a marker for anti-vascular activity

ABSTRACT: Interventions: Group 1:Patients with advanced colorectal cancer who receive a single dose of diclofenac Group3: patients with advanced colorectal cancer receiving their first dose of chemotherapy Primary outcome(s): 1. Determine if diclofenac induces a measurable rise in 5-HIAA production in patients with advanced colorectal cancer in 24hrs from administration.[];2. Compare the change in 5-HIAA induced by diclofenac and by chemotherapy in patients with advanced colorectal cancer in 24hrs from administration.[];3. Compare the change in 5-HIAA induced by diclofenac in patients with advanced colorectal cancer and in controls who do not have cancer in 24hrs from administration.[] Study Design: Purpose: Treatment; Allocation: Randomised controlled trial; Masking: Open (masking not used);Assignment: Parallel;Type of endpoint: Efficacy

DISEASE(S): Control Volunteers With No Cancer,Cancer-bowel-back Passage (rectum) Or Large Bowel (colon),Advanced Colorectal Cancer

PROVIDER: 2452276 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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Project description:Background: Colorectal cancer is the third most common and the fourth most lethal cancer in the world. In the majority of cases, patients are diagnosed at an advanced stage or even metastatic, thus explaining the high mortality. The standard protocol for treating patients with locally advanced non-metastatic colorectal cancer (CRC) is neoadjuvant radio-chemotherapy (NRCT) with 5-fluorouracil (5-FU), but the resistance rate to this treatment remains high with approximately 30% of non-responders. The lack of evidence available in clinical practice to predict NRCT resistance to 5-FU and to guide clinical practice therefore encourages the search for biomarkers of this resistance. Methods: From twenty-three formalin-fixed paraffin-embedded (FFPE) biopsies performed before NRCT with 5-FU of locally advanced non-metastatic CRC patients, we extracted and analysed the tumor proteome of these patients. From clinical data, we were able to classify the twenty-two patients in our cohort into three treatment response groups: non-responders (NR), partial responders (PR) and total responders (TR), and to compare the proteomes of these different groups. Results: We have highlighted 384 differentially expressed proteins between NR and PR, 248 between NR and TR and 417 between PR and TR. Among these proteins, we have identified many differentially expressed proteins identified as having a role in cancer (IFIT1, FASTKD2, PIP4K2B, ARID1B, SLC25A33: overexpressed in TR; CALD1, CPA3, B3GALT5, CD177, RIPK1: overexpressed in NR). We have also identified that DPYD, the main degradation enzyme of 5-FU, was overexpressed in NR, as well as several ribosomal and mitochondrial proteins also overexpressed in NR. Conclusions: From these retrospective study, we implemented a protein extraction protocol from FFPE biopsy to highlight protein differences between different response groups to RCTN with 5-FU in patients with locally advanced non-metastatic CRC. These results will pave the way for a larger cohort for better sensitivity and specificity of the signature to guide decisions in the choice of treatment.

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5HIAA as a marker for anti-vascular activity

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