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Background: Gastric cancer is the second most common cancer and known
as the second cause of death due to cancers worldwide. Adenocarcinoma is the
most fatal cancer in Iran and a patient with this kind of cancer, has a lower
lifetime than others. In this research, the survival of patients with gastric
carcinoma who were registered at Taleghani Hospital, were studied.
Methods: 291 patients with Gastric carcinoma who had received
care, chemotherapy or chemoradiotherapy, at Taleghani Hospital in Tehran from 2002 to 2007 were studied as a historical cohort. Their survival rates and its
relationship with 12 risk factors were assessed.
Results: Of the 291 patients with Gastric carcinoma, 70.1 percent were men and others (29.9%) were women. The mean age of men
was 62.26 years and of women was 59.32 years at the time of diagnosis.
Most of patients (93.91%) were advanced stage and
metastasis. The Cox proportional hazards model showed that age at diagnosis,
tumor stage and histology type with survival time had significant relationships
(p=0.039, p=0.042 and p=0.032 respectively).
Conclusion: The five-year survival rate and median lifetime of
gastric cancer patients who underwent chemotherapy or chemoradiotherapy are
very low and seems that one of the important reasons for this situation is delayed diagnosis. The
scheme of public education about the early warning signs of the disease and
diagnosis and administration of periodic examinations is unavoidable.
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Background: Seroma
formation, or the subcutaneous collection of fluid, is a common problem after
surgery for the breast cancer. It may lead to wound-related complications and
also can delay adjuvant therapy. The aim of this study was to investigate the
effect of various clinical and therapeutic variables on seroma formation.
Methods: A prospective cross sectional study of patients who
underwent surgical therapy for breast cancer was carried out. Modified radical
mastectomy was performed on 67 patients (65%) and 28 patients (27.2%) underwent breast conservative surgery. Simple
extended mastectomy was done for the remaining 8 patients (7.8%). Seroma
formation was studied in relation to age, type of surgery, tumor size, nodal
involvement, preoperative chemotherapy, surgical instrument (electrocautery or
scalpel), use of pressure garment, and duration of drainage. All of the
patients followed for 4 weeks after surgery.
Results: A total of 103 patients with breast cancer were studied. The mean
age of the patients was 48.3 years (25-82). Seroma occurred in 27 (26.2%) patients. There was
statistically significant relation between age and seroma formation after
breast cancer surgery (p=0.005), while other factors studied was found to be
significantly ineffective. In addition, there was not any relation between
seroma formation and drain duration. However, two factors including type of the
operation and level of lymphatic dissection was considerable with confidence
interval up to 90%, but it was not statistically significant with
confidence interval >95% (p=0.068 and 0.063 respectively).
Conclusion: These findings suggest that the age is a predicting
factor for seroma formation in breast cancer patients, while other factors do
not significantly affect that.
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Background: Detection rate of Ductal Carcinoma
Insitu of the breast (DCIS) have
increased rapidly over the past decade, which is generally attributed to the widespread
use of screening mammography. The aim of this study was to evaluate the prevalence
of ductal carcinoma in situ in patients who had been referred to Tehran
university medical centers.
Methods: In a retrospective study, medical
records of the patients with diagnosis of breast cancer in 3 teaching hospitals of Tehran University of
Medical Sciences (Cancer Institute, Sina and Shariati Hospitals between 1994-2003) were reviewed and records with
ductal carcinoma in situ were selected and analyzed.
Results: Between 2244 medical records of breast cancer 23 patients had DCIS (1.02%). Mean age was 47.3 years just one patient had been detected by screening mammography and
others had clinical symptoms. 48% of patients
had mass with mean size of 3.3cm. All had
undergone open biopsy (four incisional, 19 excisional). Treatment included 65.2% modified radical mastectomy, 30.4% lumpectomy with axillary dissections and 3.8% lumpectomy alone. Nine patients had radiotherapy after
surgery and ten took tamoxifen as hormonal therapy. Two patients (8.6%) in lumpectomy group had
recurrence in follow ups. Median follow up time was 84 months.
Conclusion: This study shows that the Prevalence of early stages of
breast cancer especially ductal carcinoma in situ is extremely low. (DCIS was 1.02 in comparison with 15-30% in western countries).
These findings indicate the need for increasing public information about breast
cancer in Iran and improving screening programs of breast cancer.
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Background: Gastric adenocarsinoma is the first leading fatal malignancy in Iran. Despite
advances in novel therapeutics approaches for gastric cancer (GC)
patient, tumor dissemination via blood stream to distant organ is still the
major cause of death. Therefore, there is urgent need to establish sensitive
methods for early detection of disseminated tumor cells in peripheral blood (PB)
and bone marrow (BM) specimens of gastric
cancer patients.
Methods: In the present study, we use Carcinoma Embryonic Antigen (CEA)
as a tumor marker and Glyceraldehyde 3-Phosphate
Dehydrogenase (GAPDH) as an internal
control to detection and quantification of disseminated tumor cells in PB
and BM specimens of affected individuals. Total RNA
was extracted from AGS (gastric cancer)
cell line and CEA and GAPDH
fragments were generated by reverse transcription. The amplified fragments were
cloned into pTZ57R/T vector separately.
Double cloning of these genes has done into one pTZ57R/T
vector. Serial dilution of this recombinant plasmid is used to construct
standard curve, each containing a known amount of input copy number. Total RNA
was extracted from BP and BM
specimens of 35 GC patients. cDNA
of the specimens were synthesized by reverse transcription and subjected to Quantitative
Real-Time
PCR (QRT-PCR).
Results: We developed a highly sensitive and specific quantitative PCR
for CEA and GAPDH
using Real-Time
PCR based on TaqMan
technology. CEA mRNA
was detected in 23% of PB
and 20% of BM
specimens. There was no CEA mRNA
detecting in control group.
Conclusions: The QRT-PCR for CEA
can be a useful technique for detection of micrometastases in the PB
and BM specimens of gastric cancer patients.
Normal 0 false false false EN-US X-NONE AR-SA MicrosoftInternetExplorer4 Telomere, by which is a terminal structure of eukaryotic chromosomes was discovered at first in 1938 and has a vital role in chromosome protection. Telomere in human and other vertebrates consists of thousands of 5′-TTAGGG-3′ tandem repeats at the end of the chromosome, has a main role in the chromosome stability. Telomere protects the end of the chromosome from degeneration, rearrangement and end to end fusion. There is a telomere loss at every cell division. Progressive loss in telomere length results in disassociation of telomere binding proteins and change in gene expression profiles. Adjacent genes are suppressed by the telomere effect so the telomere loss results in adjacent gene expressions. Apoptosis and replicative senescence are caused by progressive telomere loss. There are three mechanisms for increasing telomere length in eukaryotes and telomerase is the predominant mechanism. Telomerase can synthesize telomere, without the template. Telomerase is overexpressed In 90% of cancers. Therefore cancerous cells compensate the telomere loss in every cell division because of telomerase. In conclusion, telomerase is a proper target for cancer therapy and many methods including direct inhibition of telomerase and immunotherapy have been introduced.
Background: In according to immunomodulatory effect of probiotics and effect of these bacteria on the effectiveness of immune responses, at the present work we proposed the evaluation of oral administration of L.acidophilus on the immune statues in BALB/c mice bearing breast cancer.
Methods: A total of 30 In-bred BALB/c mices aged from six to eight weeks weighting 25-30g were randomly enrolled in our study, in two groups each consist of 15 mices. The L.acidophilus ATCC4356 strain used in this study was inoculated in MRS broth and cultivated for a day at 37°C under anaerobic conditions, collected by centrifugation and resuspend in Phosphate Buffer Saline (PBS). After preparation of proper amount of these suspensions it was orally administered to the mice with a gastric feeding, Control mices received an equal volume of PBS in duration of study.
Results: Results showed the increase in production of IFnγ (p<0.005), and decrease in production of Th2 cytokines such as IL4 (p=0.347) in the L.acidophilus administered mice in comparison to control group of mice. In addition the proliferation of immune cells in probiotic group was significantly higher than controls, and most importantly probiotic administered mice showed an increase in survival rate of this group compared to control mice (p<0.001).
Conclusion: Results of our study suggested that daily consumption of Lactobacillus acidophilus can regulate immune responses skewed Th1 balance that is needed against tumor, further studies is needed to investigate the other mechanisms of this effect.
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Background: Breast conservative therapy is associated with
similar outcomes in comparison with mastectomy. The
aim of this study is assessment of local recurrence rate and related risk
factors in patients who have been treated with radiotherapy after conservative
surgery for breast cancer.
Methods: This is a cohort study which data of all breast
cancer patients who have visited in follow up clinic in radiation oncology
department of cancer institute of Imam
Khomeini Hospital
complex in Tehran, Iran,
during years 2007-2009 were collected. All
of the patients were investigated for local recurrence and the possible risk
factors.
Results: Two hundred and seventy seven patients have entered
the study and all have followed for at least one year since data entry. Median
follow-up time from the start of radiotherapy were 35
months (12-148 mo).
We had seven cases (2.5%)
with local recurrences (2.5%)
which most of them occurred in first year after treatment. Because
of low rate of recurrence none of the variables such as margin and nodal status
has significant correlation with local recurrence which this should be due to
small number of patient and short time of follow up.
Conclusions: At
median follow up of 35 months from the beginning
of radiation therapy, local recurrence rate was 2.5% which
is similar to the literature. We recommend to follow a
larger group of patients for longer times to estimate recurrence risk after breast
conservative therapy.
Normal 0 false false false EN-US X-NONE AR-SA MicrosoftInternetExplorer4 Since the recognition of true number of human chromosomes in 1956, many techniques have been developed to detect chromosomal aberrations. A number of those, such as karyotyping and fluorescence in situ hybridization (FISH), are valuable tools in both research and diagnostics. But these techniques have defects that limit their application. One of the important limitations is resolution resolution limitations make it impossible to detect small aberrations. The other major defect is the disability to analyze whole genome. In 1997 Solinas-Toldo introduced a new technique that could cover other techniques' defects. This new technique called microarray-based comparative genomic hybridization (array CGH). Array CGH, with the powerful resolution of FISH and also the ability of whole genome analysis in single experiment accelerated the genetic research. Array CGH has resulted in to a great progress in oncology and genetic disorders research. In addition, this technique has the ability to be used in diagnostics too. This review article, witch include the data of recent published papers and our experiences, gives an overview of the array CGH and compare it with the other molecular cytogenetic techniques. Its application in oncology and genetic disorder is also discussed.
Background: The oncoplastic surgery has been revolutionized breast conservative surgery. The aim of our study was to represent the cosmetic outcome of oncoplastic breast surgery in Iran and to evaluate its determinants.
Methods: Fifty eight patients with unilateral breast neoplasm operated with single surgeon in Imam Khomeini Hospital, Tehran, Iran. Three view photographs were obtained pre and post operatively and were put in separate PowerPoint slides. The photographs were evaluated by six health related professionals. They scored the cosmetic outcome with modified questionnaire containing general and specific questions. Weighted kappa used for intra and inters rater reliability and ANOVA was used for analyzing cosmetic outcome determinants.Results: Generally, 72.2% of the photographs got the excellent or good score in a single breast evaluation part. Its items breast size, nipple deviation and scar quality scored 94.2, 67.9 and 88.8 respectively. "In comparison with contra-lateral breast" part shape asymmetry, need for surgery of contra lateral breast and size asymmetry scored 68.9, 75.8 and 69% respectively. Tumor size greater than two cm had poorer outcome (p=0.039) upper outer quadrant tumor had the worst and upper inner quadrant tumors had the best outcomes (p<0.0001). Patient with 50 to 60 years of age had the poorest outcomes (p<0.0001). Weighted kappa for inter and intra rater kappa was 0.12 and 0.58 respectively.
Conclusions: Acceptable cosmetic outcome is obtained in the first experience of oncoplastic breast surgery in Iran. Long term monitoring of oncologic and cosmetic outcomes in greater numbers of patients is recommended.Background: Colorectal cancer is the third common cancer world wide and the forth in Iran. Neoadjuvant chemoradiotherapy is the standard treatment for locally advanced rectal cancer. In this study we evaluate the efficacy a cox-2 inhibitor on pathologic response, sphincter preservation and acute toxicity during neoadjuvant chemoradiation.
Methods: Thirty-six patients that have adenocarcinoma of rectum was enrolled (up to 15 cm of anal verge). The patients were undergone Endometrial Ultrasound (EUS), abdomino-pelvic and chest CT for staging. Then received neoadjuvant concurrent chemo radiation (xeloda 825 mg/m2 bid in combination with celecoxib 100 mg qid and 50-50.4Gy/25-28f). Surgery was done 4-8 weeks after chemoradiation. During the chemoradiation the patients was observed for the probable complication one year. Tumor regression grade was reported.
Results: From 36 surgery patients, Total Mesorectal Excision (TME) was done in 30 patients. Pathologic complete response was seen in eight of 30 patients (26.7%). Tumor regression grade was calculated in three and five grade system: in three grade system 17 patients had grade 1 (60.7%), eight patients had grade 2 (28.6%) and three patients had grade 3 (10.7%). In five grade system of tumor regression eight patients had grade 1 (28.6%), nine patients had grade 2 (32.1%), eight patients grade 3 (28.6%), three patients had grade 4 (10.7%). T down staging was 43.3%. N downstaging was 30.8%. No patient had skin reaction or cardio-vascular complication.
Conclusion: Based on our study results, Celecoxib in combination with neoadjuvant chemoradiation is safe and is associated with low complications. This combination can promote pathologic complete response, TRG and T and N downstaging in Rectal adenocarcinoma.
Background: With approximately 386,000 deaths per year, esophageal cancer is the 6th most common cause of death due to cancer in the world. This cancer, like any other cancer, is the outcome of genetic alterations or environmental factors such as tobacco smoke and gastro-esophageal reflux. Tobacco smoking is a major etiologic factor for esophageal squamous cell carcinoma in western countries, and it increases the risk by approximately 3 to 5 folds. Chronic gastro-esophageal reflux usually leads to the replacement of squamous mucosa by intestinal-type Barrett’s metaplastic mucosa which is considered the most important factor causing esophageal adenocarcinoma. In contrast to esophageal adenocarcinoma, different risk factors and mechanisms, such as mutations in oncogenes and tumor suppressor genes, play an important role in causing esophageal squamous cell carcinoma. Molecular studies on esophageal cancers have revealed frequent genetic abnormalities in esophageal squamous cell carcinoma and adenocarcinoma, including altered expression of p53, p16, cyclin D1, EGFR, E-cadherin, COX-2, iNOS, RARs, Rb, hTERT, p21, APC, c-MYC, VEGF, TGT-α and NF-κB. Many studies have focused on the role of different polymorphisms such as aldehyde dehydrogenase 2 and alcohol dehydrogenase 2 in causing esophageal cancer. Different agents including bestatin, curcumin, black raspberries, 5-lipoxygenase (LOX) and COX-2 inhibitors have been found to play a role in inhibiting esophageal carcinogenesis. Different gene therapy approaches including p53 and p21WAF1 replacement gene therapies and therapy by suicide genes have also been experimented. Moreover, efforts have been made to use nanotechnology and aptamer technology in this regard.
Background: Human
cancer cell lines express human choriogonadotropin (hCG), its
subunits and derivatives, regardless of their origin and type. It appears that
hCG is a common phenotype in human cancer cell lines. In this research,
the effects of hCG targeting monoclonal
antibodies (7D9, T18H7 and T8B12) on
human cancer cell lines were evaluated.
Methods: Monoclonal
antibody secreting hybridomas were proliferated and injected intraperitoneally
to Balb/C mice after treatment with pristine. Two weeks later, ascites fluid
was collected. Purification of aforementioned antibodies from ascites fluid was
performed using G-protein affinity followed by
ion exchange chromatography. SDS-PAGE and ELISA
confirmed the structure and functional integrity of the purified antibodies,
respectively. Two human cancer cell lines "Hela" and "MDA"
were treated by the purified antibodies. Three days later, different wells were
imaged and the cells counted.
Results: SDS-PAGE gel
(None-reducing) indicated consistency of band migration patterns with control
antibodies. ELISA test using hCG
antigens indicated that the produced antibodies could detect hCG
antigens. Cell lines were cultured and treated with different concentrations of
each antibody. Counting and imaging different wells of treated plates,
indicated that 7D9 antibody had a more significant (P<0.01)
cytotoxic effect on cancer cell lines than the control cells.
Conclusion: HCG targeting monoclonal
antibodies can be used for targeted cancer therapy, as human cancer
cells express hCG gene. 7D9 antibody that exhibits protease activity is a
proper candidate for this purpose, as it possesses both antagonistic and
enzymatic properties.
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Background: Aldehyde
dehydrogenase 1 (ALDH1) is a marker of normal and malignant human mammary
stem cells that has been reported to be associated with poor prognosis. Studies
on the detection of ALDH1+ cells can help the treatment of patients with
breast cancer. The aim of this study was to determine the activity of ALDH1 in breast
cancer and its relationship with the pathological features of the tumors.
Methods: ALDH1 activity was studied by
immunohistochemistry in 121 paraffin-embedded histological
samples of breast cancer patients from Department of Pathology of Milad
Hospital, Tehran, Iran during 2006-2007. The
relationship of ALDH1 with the pathological features of the tumors (size,
grade, lymph node metastasis and vascular invasion) was also investigated.
Results: Eighty-five percent of breast cancer
samples expressed ALDH1 in their cytoplasm with a wide range
of intensity (weak, moderate and strong), while 18 samples (14.9%) were completely negative. The
majority of cases (97.1%) showed ALDH1 positivity in the stroma of tumors which varied from
weak (2.9%) to strong (73.5%). ALDH1 H-score (ALDH1% × intensity) of tumor cells varied from 0 to 240 (mean= 80). ALDH1 H-score was ≤80 in 62 (51.2%) and >80 in 59 (48.8%) samples. There
was no statistically significant relationship between ALDH1 H-score and age (P=0.358), tumor size (P=0.375), tumor grade (P=0.207), lymph node metastasis (P=0.125) or vascular
invasion (P=0.190).
Conclusion: ALDH1 activity was
demonstrated in 85.1% of
breast cancer samples although its level of expression was not correlated with
the pathologic features of breast tumors.
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Background: Breast
cancer is the most common form of hereditary cancer worldwide and is an
important cause of morbidity and mortality. Approximately 5-10% of breast
and ovarian cancers are
due to the highly penetrating germline mutations in cancer predisposing genes. Two genes, BRCA1 and BRCA2, account for
at least half of these cases. The demand for BRCA1 and BRCA2 mutation screening is rapidly
increasing as their identification will affect the medical management of people
at increased risk for the disease. Therefore, the aim of this study was to
investigate BRCA1/2 mutations in 100 high risk Iranian families.
Methods: One hundred families who met the
minimal risk factors for breast/ovarian cancer were screened among
the families referred to Kawsar Human Genetics Research
Center for the diseases in 2009-2011. The entire coding sequences and each
intron/exon boundaries of BRCA1/2 genes were screened for by direct
sequencing and MLPA in both patients and the controls.
Results: In the present study, we could detect
the following novel mutations:
p.Gly1140Ser, p.Ile26Val,
p.Leu1418X, p.Glu23Gln,
p.Leu3X, p.Asn1403His,
p.Asn1403Asp, p.Lys581X,
p.Pro938Arg, p.Thr77Arg,
p.Leu6Val, p.Arg7Cys,
p.Leu15Ile, p.Ser177Thr,
IVS7+83(-TT), IVS8 -70(-CATT),
IVS2+9(G>C), IVS1-20(G>A),
IVS1-8(A>G), p.Met1Ile,
IVS2+24(A>G), IVS5-8 (A>G),
IVS2(35-39)TTcctatGAT,
IVS13+9 G>C in BRCA1
and p.Glu1391Gly, p. Val1852Ile,
IVS6-70(T>G), 1994-1995
(InsA) in BRCA2.
Conclusion: Ten mutations seemed to be pathogenic and the disease-causing
mutations were seen in 16% of the families. In addition, from the
total number of substitutions and reassortments (42), 80% related to BRCA1 and 20% to mutations in BRCA2 genes.
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