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1.
Oncogene ; 29(4): 482-91, 2010 Jan 28.
Article in English | MEDLINE | ID: mdl-19881547

ABSTRACT

Both the pre-apoptotic exposure of calreticulin (CRT) and the post-apoptotic release of high-mobility group box 1 protein (HMGB1) are required for immunogenic cell death elicited by anthracyclins. Here, we show that both oxaliplatin (OXP) and cisplatin (CDDP) were equally efficient in triggering HMGB1 release. However, OXP, but not CDDP, stimulates pre-apoptotic CRT exposure in a series of murine and human colon cancer cell lines. Subcutaneous injection of OXP-treated colorectal cancer (CRC), CT26, cells induced an anticancer immune response that was reduced by short interfering RNA-mediated depletion of CRT or HMGB1. In contrast, CDDP-treated CT26 cells failed to induce anticancer immunity, unless recombinant CRT protein was absorbed into the cells. CT26 tumors implanted in immunocompetent mice responded to OXP treatment in vivo, and this therapeutic response was lost when CRT exposure by CT26 cells was inhibited or when CT26 cells were implanted in immunodeficient mice. The knockout of toll-like receptor 4 (TLR4), the receptor for HMGB1, also resulted in a deficient immune response against OXP-treated CT26 cells. In patients with advanced (stage IV, Duke D) CRC, who received an OXP-based chemotherapeutic regimen, the loss-of-function allele of TLR4 (Asp299Gly in linkage disequilibrium with Thr399Ile, reducing its affinity for HMGB1) was as prevalent as in the general population. However, patients carrying the TLR4 loss-of-function allele exhibited reduced progression-free and overall survival, as compared with patients carrying the normal TLR4 allele. In conclusion, OXP induces immunogenic death of CRC cells, and this effect determines its therapeutic efficacy in CRC patients.


Subject(s)
Antineoplastic Agents/therapeutic use , Apoptosis/drug effects , Colonic Neoplasms/drug therapy , Colonic Neoplasms/immunology , Organoplatinum Compounds/therapeutic use , Aged , Animals , Calreticulin/genetics , Calreticulin/metabolism , Cell Line, Tumor , Cisplatin/pharmacology , Colonic Neoplasms/genetics , Colonic Neoplasms/pathology , Female , HMGB1 Protein/immunology , HMGB1 Protein/metabolism , Humans , Male , Mice , Mice, Inbred BALB C , Middle Aged , Neoplasm Staging , Neoplasm Transplantation , Oxaliplatin , Polymorphism, Genetic , Prognosis , Toll-Like Receptor 4/deficiency , Toll-Like Receptor 4/immunology
2.
Eur J Surg Oncol ; 36(3): 324-8, 2010 Mar.
Article in English | MEDLINE | ID: mdl-19959323

ABSTRACT

BACKGROUND: Hyperthermic intraperitoneal chemotherapy (HIPEC) is a complex, expensive and time-consuming procedure. Despite its good results in the treatment of peritoneal carcinomatosis, these factors have precluded the wider use of this procedure around the world. We hypothesized that HIPEC could be performed by heating the liquid within the abdomen and thus avoiding the need for an external heating circuit and a pump. The aim of this study was to assess the feasibility and safety of an internal heating device for hyperthermic intraperitoneal chemotherapy in an experimental model. METHODS: Four large-white pigs underwent one-hour open intraperitoneal hyperthermia with closed abdomen using this new device. Constant stirring of the liquid around the viscera was performed in the first three animals, but not in the fourth one. At the end of the procedure, all of the viscera were carefully examined to look for thermal injury. Any lesion or doubtful area was removed and sent to pathologic examination. RESULTS: No adverse events occurred during surgery in any of the animals. A temperature of 42 degrees C was reached in an average time of 14 min and maintained homogeneously between 42 degrees C and 43 degrees C for one hour. No visceral injury was detected in the first three animals. Three foci of thermal injury to the mucosa were detected in the absence of stirring (fourth animal). CONCLUSION: Heating the solution within the abdomen during hyperthermic intraperitoneal chemotherapy is feasible, safe and achieves perfect thermal homogeneity. This device provides a time-saving inexpensive way to perform intraperitoneal hyperthermic chemotherapy.


Subject(s)
Antineoplastic Agents/administration & dosage , Carcinoma/therapy , Hyperthermia, Induced/instrumentation , Neoplasms, Experimental/therapy , Peritoneal Neoplasms/therapy , Animals , Equipment Design , Feasibility Studies , Female , Injections, Intraperitoneal , Swine , Treatment Outcome
4.
J Cancer Res Clin Oncol ; 131(8): 504-10, 2005 Aug.
Article in English | MEDLINE | ID: mdl-15902487

ABSTRACT

PURPOSE: The present study was designed to determine whether the nuclear or cytoplasmic expression of survivin, was related to clinicopathological parameters and survival in sporadic colon carcinomas. METHODS: Western blotting of cell fractions and immunocytochemical methodology were used in five human colon cancer cell lines. Immunohistochemical study was performed in formalin-fixed paraffin-embedded section from 46 patients with sporadic colorectal adenocarcinomas with a polyclonal antibody directed against survivin. Apoptotic index was evaluated by using the M30 antibody. Survival rates were estimated by the Kaplan-Meier method and compared using the log-rank test. Multivariate survival analysis was performed by the Cox proportional hazards model. RESULTS: Western blotting and immunocytochemistry analyses confirmed that survivin could be detected both in the nucleus and the cytoplasm. Immunohistochemical analysis demonstrated that 39% of tumours expressed survivin in the nucleus and 41% in the cytoplasm. No relationship was observed between survivin expression and clinicopathological features. Unexpectedly, the apoptotic index appeared to be linked with high survivin nuclear expression. Overall, 3-year observed survival rate was 73% in patients with cytoplasmic survivin expression versus 48% for negative expression (P = 0.14). Survival was 72% versus 50% for positive nuclear survivin expression versus negative (P = 0.16). After adjustment for age and stage, cytoplasmic survivin expression was a significant prognostic factor. A high level of expression was associated to a better survival: RR = 0.35 [0.13-0.98], P = 0.045. CONCLUSION: These results indicate that the analysis of the subcellular expression of survivin is a determining factor to define the prognostic value. Its evaluation, using a polyclonal antibody, might help clinicians in the stratification of patients with colorectal cancer.


Subject(s)
Biomarkers, Tumor/analysis , Carcinoma/chemistry , Colonic Neoplasms/chemistry , Microtubule-Associated Proteins/analysis , Neoplasm Proteins/analysis , Aged , Apoptosis , Blotting, Western , Carcinoma/pathology , Colonic Neoplasms/pathology , Female , Humans , Immunohistochemistry , Inhibitor of Apoptosis Proteins , Male , Multivariate Analysis , Predictive Value of Tests , Prognosis , Proportional Hazards Models , Survival Analysis , Survivin
5.
Am J Surg Pathol ; 28(12): 1553-9, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15577673

ABSTRACT

The assessment of the microsatellite instability (MSI) status in colorectal cancers is presently warranted for three reasons: 1) as a screening tool for hereditary nonpolyposis colorectal cancer, 2) as a prognostic marker, and 3) as a potential predictive factor of chemotherapy response. The aim of this study was to evaluate, on a large scale with tissue samples coming from a number of different sources, the difficulties met with routine use of immunohistochemistry (IHC) and to determine if it really does offer an accurate alternative to PCR genotyping. Colorectal carcinomas from 462 consecutive patients resected in public or private hospitals were assessed for MSI status by two methods: MSI testing (with BAT-26 microsatellite) and IHC detection of hMLH1, hMSH2, and hMSH6 proteins. Of the 398 cancers tested, immunohistochemistry was noncontributory in 42 (10.5%), focal in 9 (2.3%), and discordant with the PCR results in 36 (9%). For these 87 cases, complementary analyses were performed to explain discrepancy. After additional IHC assay with modified processing protocols, 8 cases remained noncontributory, 2 focal, and 28 discordant: 18 microsatellite stability IHC/MSI PCR and 10 MSI IHC/microsatellite stability PCR. For these discordant cases, we performed a multiplex PCR assay on DNA extracted from the frozen sample and BAT-26 was amplified from DNA extracted from the paraffin blocks used for IHC. Four discordant cases were reclassified after PCR multiplex assay (3 as MSI and 1 as microsatellite stability). Five other cases displayed intratumoral heterogeneity and 19 remained discordant. The discrepancy could be partly explained by variable technical protocols of fixation in the different laboratories, leading to variations in staining quality and difficulties in IHC interpretation. This population-based study is the first one to show that IHC is not sensitive and specific enough to be used routinely. Immunohistochemistry analysis of MMR proteins must be performed in standardized conditions and interpreted by confirmed pathologists. It cannot replace PCR as long as protocols are not optimized and harmonized.


Subject(s)
Colorectal Neoplasms/genetics , Immunohistochemistry , Microsatellite Repeats/genetics , Polymerase Chain Reaction , Aged , Female , Humans , Male , Prognosis , Sensitivity and Specificity
6.
Dis Colon Rectum ; 47(3): 323-33, 2004 Mar.
Article in English | MEDLINE | ID: mdl-14991494

ABSTRACT

PURPOSE: The identification of groups with a high risk of colorectal adenoma recurrence remains a controversial issue for clinicians. This study was designed to assess the predictive value of initial patient and adenoma characteristics of the three-year recurrence. METHODS: The study population was composed of 552 patients with resected colorectal adenomas who completed the European Fiber-Calcium Intervention trial. At both baseline and three-year examinations, the characteristics of adenomas were recorded according to a standardized protocol. The main outcomes measured were the three-year overall recurrence, recurrence of multiple adenomas, recurrence of advanced adenomas (size > or = 1 cm or tubulovillous/villous architecture or moderate/severe dysplasia), and proximal and distal recurrence. RESULTS: A three-year recurrence was observed in 122 patients (22.1 percent), and more than one-half of them had recurrent adenomas on the proximal colon. After adjustment for patient characteristics and treatment allocation, the number of adenomas and their proximal location at baseline were the main predictors of recurrence. In comparison with patients who had one or two adenomas on the distal colon, patients with three or more adenomas with at least one of them located on the proximal colon had a much higher risk of overall recurrence (5.3; 95 percent confidence interval, 2.7-10.3), proximal recurrence (8.5; 95 percent confidence interval, 4.1-18), and advanced adenoma recurrence (5.5; 95 percent confidence interval, 2.4-12.6). CONCLUSIONS: Follow-up colonoscopies in patients with adenomas should include careful examination of the proximal colon. The time interval between follow-up examinations could probably be extended beyond three years in patients who have only one or two distal adenomas.


Subject(s)
Adenoma/pathology , Colorectal Neoplasms/pathology , Neoplasm Recurrence, Local/pathology , Adenoma/surgery , Colon/pathology , Colonoscopy , Colorectal Neoplasms/surgery , Double-Blind Method , Europe/epidemiology , Female , Humans , Male , Middle Aged , Multivariate Analysis , Neoplasm Recurrence, Local/epidemiology , Predictive Value of Tests , Risk Factors
7.
Int J Radiat Biol ; 79(10): 787-92, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14630537

ABSTRACT

Structural changes that might influence the structural integrity of the vessel in response to intravascular brachytherapy (IVB) and stenting were examined, focus being on the importance of neovascularization in rabbit stented arteries. Stents were implanted in the infrarenal aortas of rabbits, immediately followed by gamma IVB or a sham radiation procedure, and the arteries harvested at 6 months. Labelling for von Willebrand factor showed an increase in adventitial and medial neovascularization in irradiated versus control arteries group (5.04+/-0.89 versus 1.51+/-0.23 mm(-2), respectively; p=0.004). Moreover, intramedial haemorrhages (free hemosiderin deposition) and inflammation (macrophages) were only observed in irradiated arteries. No significant change in expression of matrix metalloproteinase 1, 2 or 3 was observed between the irradiated and control group while collagen content decreased in the irradiated versus the control group (10.05%+/-1.48% versus 31.92%+/-3.12%, respectively; p<0.001). The study supports the hypothesis that IVB associated with stenting induces late deleterious effects on the medial layer, characterized by formation of intramural neovessels, haemorrhages and a decrease in collagen content.


Subject(s)
Aorta, Abdominal/pathology , Aorta, Abdominal/radiation effects , Brachytherapy/adverse effects , Hemorrhage/etiology , Neovascularization, Pathologic/etiology , Stents/adverse effects , Vascular Diseases/etiology , Animals , Aorta, Abdominal/metabolism , Aorta, Abdominal/surgery , Collagen/metabolism , Coronary Restenosis/prevention & control , Coronary Restenosis/radiotherapy , Gamma Rays/adverse effects , Hemorrhage/metabolism , Hemorrhage/pathology , Male , Metalloproteases/metabolism , Rabbits , Reference Values , Vascular Diseases/metabolism , Vascular Diseases/pathology
8.
Histopathology ; 43(1): 40-7, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12823711

ABSTRACT

AIMS: The aim of this study was to assess the independent value of pathological criteria in the diagnosis of mismatch repair (MMR)-defective sporadic colorectal cancers. METHODS AND RESULTS: Resected colorectal adenocarcinomas (n = 273) were reviewed in order to identify a number of specific morphological features of MMR-defective carcinomas. Of the 273 cases, 35.2% were right-sided and 5.9% were poorly differentiated. Focal extracellular mucin secretion was seen in 5.1% of cases and a stromal follicular reaction in 4.6%. The expression of the two major MMR proteins hMLH1 and hMSH2 was studied by immunohistochemistry. Carcinomas were considered deficient in the MMR system when a loss of nuclear signal in neoplastic cells was observed for one of the proteins. Such an extinction was seen in 37 of the cases (13.6%). The hMLH1 protein was the one most frequently altered (86.5%). After multivariate analysis, three independent factors were significantly associated with MMR deficiency: proximal location [odds ratio (OR) = 9.30; 95% confidence interval (CI) 2.79, 30.98], the presence of a true stromal follicular reaction (OR = 13.60; 95% CI 2.98, 62.00) and poor differentiation (OR = 8.33; 95% CI 1.63, 40.32). CONCLUSIONS: These results confirm that sporadic colorectal MMR-defective adenocarcinomas display certain specific morphological characteristics. However, these pathological features are not sufficiently predictive and immunohistochemistry is needed to identify such tumours accurately.


Subject(s)
Adenocarcinoma/genetics , Base Pair Mismatch , Colorectal Neoplasms/genetics , DNA-Binding Proteins , Neoplasm Proteins/genetics , Proto-Oncogene Proteins/genetics , Adaptor Proteins, Signal Transducing , Adenocarcinoma/metabolism , Adenocarcinoma/pathology , Adult , Aged , Aged, 80 and over , Biomarkers, Tumor/metabolism , Carrier Proteins , Colorectal Neoplasms/metabolism , Colorectal Neoplasms/pathology , DNA, Neoplasm/analysis , Female , Humans , Immunoenzyme Techniques , Male , Microsatellite Repeats , Middle Aged , Mucins/metabolism , MutL Protein Homolog 1 , MutS Homolog 2 Protein , Neoplasm Proteins/metabolism , Neoplasm Staging , Nuclear Proteins , Proto-Oncogene Proteins/metabolism , Retrospective Studies , Stromal Cells/metabolism , Stromal Cells/pathology
9.
Br J Cancer ; 87(4): 400-4, 2002 Aug 12.
Article in English | MEDLINE | ID: mdl-12177776

ABSTRACT

Microsatellite instability has been proposed as an alternative pathway of colorectal carcinogenesis. The aim of this study was to evaluate the interest of immunohistochemistry as a new tool for highlighting mismatch repair deficiency and to compare the results with a PCR-based microsatellite assay. A total of 100 sporadic proximal colon adenocarcinomas were analysed. The expression of hMLH1, hMSH2 and hMSH6 proteins evaluated by immunohistochemistry was altered in 39% of the cancers, whereas microsatellite instability assessed by PCR was detected in 43%. There was discordance between the two methods in eight cases. After further analyses performed on other tumoural areas for these eight cases, total concordance between the two techniques was observed (Kappa=100%). Our results demonstrate that immunohistochemistry may be as efficient as microsatellite amplification in the detection of unstable phenotype provided that at least two samples of each carcinoma are screened, because of intratumoural heterogeneity.


Subject(s)
Adenosine/genetics , Colonic Neoplasms/genetics , DNA Repair , DNA-Binding Proteins , Immunohistochemistry , Microsatellite Repeats , Mutation , Adaptor Proteins, Signal Transducing , Base Pair Mismatch , Carrier Proteins , Female , Humans , Male , MutL Protein Homolog 1 , MutS Homolog 2 Protein , Neoplasm Proteins/genetics , Nuclear Proteins , Polymerase Chain Reaction , Proto-Oncogene Proteins/genetics
12.
Pathol Biol (Paris) ; 49(2): 115-23, 2001 Mar.
Article in French | MEDLINE | ID: mdl-11317955

ABSTRACT

Mutations of the p53 gene are the most common genetic alteration in malignant human tumors. A cyclin-dependent kinase inhibitor, p21WAF1/CIP1, is thought to be an important mediator of p53-induced cell cycle arrest. Although numerous studies have reported p53 expression and mutation in colorectal cancer few of them have correlated p53 expression with that of its downstream effector p21 and with the proliferation index as measured by expression of the Ki67 nuclear antigen. We studied p53, p21 and Ki67 expression by immunohistochemistry and molecular biology in 35 colorectal carcinomas. We compared these findings with each other and with clinical factors. Sixty three percent of tumors expressed p53 whereas seventy one percent expressed p21WAF1/CIP1. In adenocarcinomas, p21 staining was heterogeneous: p21-reactive cells were seen in the most differentiated areas. There was no correlation between p21WAF1/CIP1 and p53 expression, p53 mutation, Ki67 expression or clinical factors such as sex or location of the tumor. On the other hand, there was a statistical relationship between p21 expression and survival: our results indicated an association between high p21 expression and lower stages p21WAF1/CIP1 appears to be induced independently of p53 in these tumors and may be associated with differentiation rather than proliferation.


Subject(s)
Adenocarcinoma/genetics , Biomarkers, Tumor/biosynthesis , Colorectal Neoplasms/genetics , Cyclins/biosynthesis , Genes, p53 , Ki-67 Antigen/genetics , Neoplasm Proteins/biosynthesis , Adenocarcinoma/metabolism , Adult , Aged , Biomarkers, Tumor/genetics , Colorectal Neoplasms/metabolism , Cyclin-Dependent Kinase Inhibitor p21 , Cyclins/genetics , Humans , Ki-67 Antigen/biosynthesis , Middle Aged , Neoplasm Proteins/genetics , Pilot Projects , Polymerase Chain Reaction , Polymorphism, Single-Stranded Conformational , Prospective Studies
13.
Hum Pathol ; 32(3): 320-6, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11274642

ABSTRACT

Wegener's granulomatosis (WG) is an inflammatory, destructive, angiotropic lesion. The inflammatory process involves accumulation of macrophages, lymphocytes, and polymorphonuclear neutrophils. We studied 6 lung biopsy specimens from patients with WG to characterize the cellular infiltrate and to analyze the mechanism of immune cell recruitment. We show that lymphocytes accumulating in WG lesions are mostly memory CD4(+)CD45RO(+) T lymphocytes and, although less numerous, CD8(+)CD45RO(+) T lymphocytes. Few if any B lymphocytes or natural killer cells are present within lesions. The chemokine RANTES (regulated upon activation in normal T cells, expressed and secreted) has been reported to recruit memory T lymphocytes and macrophages selectively. We used reverse-transcription polymerase chain reaction, in situ hybridization, and immunohistochemistry to study its production in WG. RANTES was expressed at a higher level in WG lungs than in normal controls, especially around microabscesses. As visualized immunohistochemically in serial sections with anti-RANTES monoclonal antibody, RANTES production was produced mainly by macrophages. Expression of the gene coding for interferon-gamma (IFN-gamma), a potent RANTES inducer, was also studied. Its expression was also much stronger in WG than in controls. Our observations are consistent with a cascade of events leading to the recruitment of immune cells in WG, sequentially involving production of IFN-gamma by T lymphocytes and RANTES production by macrophages, leading to the homing of memory T-helper lymphocytes and macrophages. HUM PATHOL 32:320-326.


Subject(s)
Chemokine CCL5/genetics , Gene Expression , Granulomatosis with Polyangiitis/metabolism , Lung Diseases/metabolism , Adult , Aged , Antibodies, Monoclonal , B-Lymphocytes/chemistry , B-Lymphocytes/pathology , Biopsy , CD4-Positive T-Lymphocytes/chemistry , CD4-Positive T-Lymphocytes/pathology , Chemokine CCL5/analysis , Female , Granulomatosis with Polyangiitis/pathology , Humans , Immunohistochemistry , In Situ Hybridization , Interferon-gamma/genetics , Leukocyte Common Antigens/analysis , Lung Diseases/pathology , Macrophages/chemistry , Macrophages/metabolism , Macrophages/pathology , Male , Middle Aged , Reverse Transcriptase Polymerase Chain Reaction , T-Lymphocytes/chemistry , T-Lymphocytes/pathology
14.
J Clin Oncol ; 19(1): 253-9, 2001 Jan 01.
Article in English | MEDLINE | ID: mdl-11134220

ABSTRACT

PURPOSE: In patients with neutropenia, thoracic computed tomography (CT) halo and air-crescent signs are recognized as major indicators of invasive pulmonary aspergillosis (IPA). Nevertheless, the exact timing of CT images is not well known. PATIENTS AND METHODS: Seventy-one thoracic CT scans were analyzed in 25 patients with neutropenia with surgically proven IPA. RESULTS: On the first day of IPA diagnosis with early CT scan (d0), a typical CT halo sign was observed in 24 of 25 patients. At that time, the median number of thoracic lesions was two (range, one to six), and pulmonary involvement was bilateral in 12 cases. The halo sign was present in 68%, 22%, and 19% of cases on d3, d7, and d14, respectively. Similarly, the air-crescent sign was seen in 8%, 28%, and 63% of cases on the same days. Otherwise, a nonspecific air-space consolidation aspect was seen in 31%, 50%, and 18% of cases on the same days. The analysis of calculated aspergillary volumes on CT showed that, despite antifungal treatment, the median volume of lesions increased four-fold from d0 to d7, whereas it remained stable from d7 to d14. Overall, 21 patients (84%) were cured by the medical-surgical approach. CONCLUSION: In patients with neutropenia, CT halo sign is a highly effective modality for IPA diagnosis. The duration of the halo sign is short, and it demonstrates the value of early CT. The increase of the aspergillosis size on CT in the first days after IPA diagnosis is not correlated with a pejorative immediate outcome when using a combined medical-surgical approach.


Subject(s)
Aspergillosis/diagnostic imaging , Hematologic Neoplasms/microbiology , Lung Diseases, Fungal/diagnostic imaging , Neutropenia/microbiology , Tomography, X-Ray Computed , Adolescent , Adult , Aged , Aspergillosis/etiology , Aspergillosis/therapy , Aspergillus/growth & development , Child , Child, Preschool , Hematologic Neoplasms/complications , Humans , Lung Diseases, Fungal/etiology , Lung Diseases, Fungal/therapy , Middle Aged , Neutropenia/etiology , Statistics, Nonparametric
15.
Rev Mal Respir ; 18(6 Pt 1): 657-60, 2001 Dec.
Article in French | MEDLINE | ID: mdl-11924189

ABSTRACT

Post-traumatic fat embolism was disclosed by a picture of alveolar hemorrhage. Acute hypoxemia associated with dense bilateral pulmonary infiltrates was observed in a 21 year-old woman, 4 days after an accident with closed tibial fracture. Cruoric pulmonary thromboembolism was ruled out, as was an acute pulmonary edema. Neither infectious nor immunologic etiology was found. The diagnosis of alveolar hemorrhage was based on bronchoalveolar lavage. Lipid droplets in macrophages stained by "Oil Red O" established the relationship with fat embolism. The outcome was favorable. The association of fat embolism and alveolar hemorrhage has already been reported, but remains rare.


Subject(s)
Embolism, Fat/complications , Hemorrhage/etiology , Pulmonary Alveoli , Adult , Female , Humans , Lung Diseases/etiology
17.
Eur J Cancer Prev ; 8 Suppl 1: S13-20, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10772413

ABSTRACT

Molecular studies have shown that different genetic pathways are involved in the history of colorectal carcinomas. This suggests that a correlation exists between the molecular, clinical and pathological features of tumours. Two large groups can be individualized: the first group is characterized by allelic losses and hyperdiploidy. These LOH (for loss of heterozygosity)-positive tumours represent 80% of colorectal carcinomas. Among them more than two-thirds are located in the distal colon. They have the worst prognosis. The second group has a normal diploid pattern and a phenotypic microsatellite instability without allelic losses. These tumours represent 10-15% of all colorectal carcinomas and about 30% of the right-sided tumours. They are associated with a better prognosis. In the future, it would perhaps be better to classify colorectal carcinomas according to their molecular features rather than to their topographical localizations.


Subject(s)
Carcinoma/genetics , Carcinoma/pathology , Colorectal Neoplasms/genetics , Colorectal Neoplasms/pathology , Genes, p53/genetics , Genetic Predisposition to Disease , Carcinoma/epidemiology , Colorectal Neoplasms/epidemiology , Female , Genetic Markers , Humans , Incidence , Male , Microsatellite Repeats/physiology , Mutation , Prognosis , Risk Factors , Sensitivity and Specificity , Survival Rate
19.
Ann Pathol ; 18(5): 444-9, 1998 Nov.
Article in French | MEDLINE | ID: mdl-9864586

ABSTRACT

The purpose of these recommendations is to provide an informative report for the clinician. The recommendations have been divided into two major areas 1) a standardized form, 2) items that provide an informative gross description and diagnostic features that are recommended to be included in every report. In special circumstances, the recommendations may not be applicable.


Subject(s)
Colorectal Neoplasms/pathology , Forms and Records Control , Pathology, Clinical , Colorectal Neoplasms/classification , Humans , Lymph Nodes/pathology
20.
Histopathology ; 33(4): 304-10, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9822918

ABSTRACT

AIMS: There is controversy over the value of the pathological classifications of gastric carcinomas in the prediction of patient survival. This study was designed to assess the prognostic value of four widely used pathological classifications, in addition to classical prognostic factors. METHODS AND RESULTS: Records from the population-based registry of digestive tract tumours in the department of Côte d'Or (France) have been analysed. All available histopathological slides of gastric cancer resected between 1976 and 1985 were reviewed and classified according to World Health Organization (WHO), Laurén, Ming and Goseki pathological coding systems. A relative survival analysis was performed using a relative survival model with proportional hazard applied to net mortality by interval. WHO, Laurén or Goseki classifications were not found to be independent prognostic factors. In addition to advanced age group, depth of parietal involvement, nodal involvement, presence of metastases, tumour site and gross appearance of the tumour, the Ming's infiltrative type was associated with a lower survival. CONCLUSION: This study suggests an independent prognostic value of the Ming subtypes with respect to survival in patients resected for gastric carcinoma.


Subject(s)
Carcinoma/pathology , Stomach Neoplasms/pathology , Adult , Aged , Aged, 80 and over , Carcinoma/mortality , Female , Humans , Male , Middle Aged , Multivariate Analysis , Prognosis , Risk , Stomach Neoplasms/mortality , Survival Rate
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