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Surgical peritoneal stress creates a pro-metastatic niche promoting resistance to apoptosis via IL-8
by
Pasquier, Jennifer
, Bonneau, Claire
, Vidal, Fabien
, Hoarau-Véchot, Jessica
, Touboul, Cyril
, Daraï, Emile
, Rafii, Arash
in
AKT protein
/ Animal models
/ Apoptosis
/ Autocrine signalling
/ Biomedical and Life Sciences
/ Biomedicine
/ Biopsy
/ Cancer cells
/ Cancer microenvironment
/ Cancer therapies
/ Chemoresistance
/ Chemotherapy
/ Cytokines
/ IL8
/ Interleukin 8
/ Laboratories
/ Malignancy
/ Medicine/Public Health
/ Metastases
/ Metastasis
/ Ovarian cancer
/ Paclitaxel
/ Patients
/ Peritoneum
/ Surgery
/ Tumor cell lines
/ Tumor microenvironment
2018
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Surgical peritoneal stress creates a pro-metastatic niche promoting resistance to apoptosis via IL-8
by
Pasquier, Jennifer
, Bonneau, Claire
, Vidal, Fabien
, Hoarau-Véchot, Jessica
, Touboul, Cyril
, Daraï, Emile
, Rafii, Arash
in
AKT protein
/ Animal models
/ Apoptosis
/ Autocrine signalling
/ Biomedical and Life Sciences
/ Biomedicine
/ Biopsy
/ Cancer cells
/ Cancer microenvironment
/ Cancer therapies
/ Chemoresistance
/ Chemotherapy
/ Cytokines
/ IL8
/ Interleukin 8
/ Laboratories
/ Malignancy
/ Medicine/Public Health
/ Metastases
/ Metastasis
/ Ovarian cancer
/ Paclitaxel
/ Patients
/ Peritoneum
/ Surgery
/ Tumor cell lines
/ Tumor microenvironment
2018
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Surgical peritoneal stress creates a pro-metastatic niche promoting resistance to apoptosis via IL-8
by
Pasquier, Jennifer
, Bonneau, Claire
, Vidal, Fabien
, Hoarau-Véchot, Jessica
, Touboul, Cyril
, Daraï, Emile
, Rafii, Arash
in
AKT protein
/ Animal models
/ Apoptosis
/ Autocrine signalling
/ Biomedical and Life Sciences
/ Biomedicine
/ Biopsy
/ Cancer cells
/ Cancer microenvironment
/ Cancer therapies
/ Chemoresistance
/ Chemotherapy
/ Cytokines
/ IL8
/ Interleukin 8
/ Laboratories
/ Malignancy
/ Medicine/Public Health
/ Metastases
/ Metastasis
/ Ovarian cancer
/ Paclitaxel
/ Patients
/ Peritoneum
/ Surgery
/ Tumor cell lines
/ Tumor microenvironment
2018
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Surgical peritoneal stress creates a pro-metastatic niche promoting resistance to apoptosis via IL-8
Journal Article
Surgical peritoneal stress creates a pro-metastatic niche promoting resistance to apoptosis via IL-8
2018
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Overview
Background
The mainstay of treatment of advanced ovarian cancer (AOC) involves chemotherapy, and debulking surgery. However, despite optimal surgical procedure and adjuvant chemotherapy, 60% of patients with AOC will relapse within 5 years. Most recurrences occur in the peritoneal cavity, suggesting the existence of occult sanctuaries where ovarian cancer cells (OCC) are protected. In murine models, surgical stress favors tumor growth; however, it has never been established that surgery may affect OCC sensitivity to subsequent chemotherapy. In this study, we investigated how the surgical stress could affect the chemosensitivity of OCC.
Methods
To avoid bias due to tumor burden in peritoneal cavity and duration of surgery, we used peritoneal biopsies from patients without a malignancy at precise time points. During laparotomies, peritoneal biopsies at the incision site were performed at the time of incision (H0 sample) and 1 h after initiation of surgery (H1 sample). We evaluated the chemoresistance to Taxol (0–20 µM) induced by H0 or H1 incubation (24 h) in two ovarian cancer cell lines OVCAR3 and SKOV3 and a primary cancer cell lines derived in our laboratory.
Results
Our results indicate that stressed peritoneum overexpressed cytokines, resulting in OCC increased resistance to therapy. Among these cytokines, IL8 was responsible for the resistance to apoptosis through the AKT pathway activation. Chemoresistance in OCC persists through the establishment of an autocrine IL8 loop. Finally, in a cohort of 32 patients, we showed an impact of IL8 tumoral overexpression on chemosensitivity and survival outcomes with a significant association to earlier recurrence.
Conclusions
Our study demonstrated that precision surgery where targeted treatment would be used in combination with surgery is essential to obtain better tumor control.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
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