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CONTENTS
No.
|
Titles /
Authors /Abstracts
|
Full Text
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No.
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1
|
Prognostic and predictive value
of excision repair cross-complementation group-1protein
expression in locally advanced bladder cancer
Wael Mansour1, Walid Almorsy1 and Maha
shamloula2
Clinical Oncology Department, Histopathology Department Faculty
of Medicine, Tanta University,
Gharbia, Egypt.
walidaa1@hotmail.com
Abstract:
Background:
A viable treatment option for locally advanced bladder cancer
includes tri-modality therapy with a combination of
transurethral resection of bladder tumor (TURBT), chemotherapy
and radiation therapy.
Cisplatin is the most important chemotherapeutic agent for
locally advanced bladder cancer and is usually administered with
Gemcitabine. Increased
expression of excision repair cross-complementation group 1
(ERCC1) protein is associated with resistance to cisplatin-based
chemotherapy in various tumor types.
The aim of the present study was to assess the prognostic and
predictive value of (ERCC1) protein in locally advanced bladder
cancer patients who received cisplatin-based chemotherapy.
Patients and Methods:
Seventy eight
patients with non-metastatic locally advanced bladder cancer
were included in this study
between
June 2013
and
December 2014. Paraffin blocks
obtained from all patients were analyzed for ERCC1 in
immunohistochemical expression.
Results:
Complete response rate was higher in patients with negative
ERCC1 expression (94.1%) than weak, moderate and strong positive
(70%, 50%& 33.3% respectively) which was statistically
significant (P= 0.019). The 2-year disease-free survival rates
for patients with ERCC1-weak positive was 40%, while it was
16.7% in moderate +ve ERCC1-, and 0% in strong +ve ERCC1,
however, it was 70% in ERCC1-negative patients. The interaction
term between ERCC1 expression and adjuvant platinol based
chemotherapy showed significance for
overall survival (P = 0.001) and
disease-free survival (P = 0.01).
Conclusion:
ERCC1appear to be potentially useful prognostic and predictive
markers in non-metastatic locally advanced bladder cancer.
[Wael
Mansour, Walid Almorsy and Maha shamloula.
Prognostic and predictive Valueofexcision
repair cross-complementation group-1protein
expression in locally advanced bladder cancer. Cancer Biology 2016;6(4):1-8].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
1. doi:10.7537/marscbj060416.01.
Key words:
locally advanced bladder cancer, ERCC1, cisplatin-based
chemotherapy, prognosis. |
Full Text |
1
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2
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Integration of Neoadjuvant Chemotherapy and Interval Debulking
Surgeries in Patients with Advanced Epithelial Ovarian Cancer
Loaie El-Helw 1,2, Abeda Raiyan1,
Rajanee Bhana1
1
The Cancer Centre, the Royal Stoke University Hospital,
Stoke-on-Trent, UK
2
The Department of Internal Medicine, the Medical Oncology Unit,
Mansoura University, Mansoura, Egypt
loaieelhelw@hotmail.com,
loaie.elhelw@uhns.nhs.uk
Abstract:
Neoadjuvant chemotherapy (NAC) and interval debulking surgery
(IDS) after 3 NAC cycles is an acceptable approach to achieve
optimal cytoreduction in patients with advanced epithelial
ovarian cancer (AEOC) who are not candidate for primary
debulking surgery (PDS). The best timing of cytoreductive
surgery and the role of late debulking surgery (LDS) after 6
cycles of NAC are still unclear. We aimed to study the outcome
of such patients who were treated in our centre in the Royal
Stoke University Hospital, Stoke-On-Trent between July 2009 and
July 2014. One hundred and eight patients with AEOC were
treated under our gynaecology oncology team during that period.
Sixty six patients (61.1%) were in stages III and 42 (38.9%) in
stage IV. All patients received NAC; 64 patients (59.3%) had
paclitaxel and carboplatin regimen and 44 (40.7%) single agent
carboplatin. Response to chemotherapy was assessed after 2
cycles; 81 patients (75%) had partial response, 21 (19.4%)
stable disease and 6 (5.6%) progressive disease. Forty one
patients (38%) proceeded to IDS after cycle 3 and 11 patients
(10.2%) to LDS after cycle 6 but 56 (51.9%) had no debulking
surgery (NDS). After a median follow up period of 18 months
(range 6-84 months), 95 patients (88%) had relapsing/progressive
disease. The median PFS durations were 13 and 12 months for
patients who had either IDS and LDS respectively compared to 8
months for NDS. The 2 years PFS probabilities were 18% for
patients who had IDS, 15% for LDS compared to 0% for NDS (P
0.000 Log rank test). The median overall survival (OS) durations
were 48, 33 and 18 months for patients who had IDS, LDS and NDS
respectively. The 2 years OS probabilities were 75% for patients
who had either IDS, or LDS compared to 38% for NDS (P.000 Log
rank test). In our study, we documented PFS and OS advantages
for patients who IDS or LDS compared to NDS and therefore should
be considered whenever possible as part of the primary treatment
of AEOC patients. Interval debulking surgery (IDS) offers longer
duration and higher probabilities of PFS and OS compared to LDS.
More patients-therefore- should be selected for IDS. There is a
need for improving NAC possibly with integrating target agents
and the use of more intensified schedules.
[Loaie
El-Helw, Abeda Raiyan,
Rajanee Bhana. Integration of Neoadjuvant
Chemotherapy and Interval Debulking Surgeries in Patients with
Advanced Epithelial Ovarian Cancer.
Cancer Biology
2016;6(4):9-15].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
2. doi:10.7537/marscbj060416.02.
Key words:
advanced ovarian cancer-neoadjuvant chemotherapy-surgical
debulking. |
Full Text |
2
|
3
|
Demographic and genetic study
for a sample of Iraqi smokers
Bushra jasim Mohammed 1,
Amina N. AL-Thwani 1,
Raghuraman Kannan
2
1.
Institute of genetic engineering and biotechnology, University
of Baghdad, Iraq
2.
University of Missouri/Colombia, USA
bbushra880@gmail.com
Abstract:
Abstract:
To examine the relationship between smoking and genetic and
demographic aspects, using statistical analysis and genetic
techniques. Subjects and methods:
One hundred and fifty of
apparently
healthy
Iraqi heavy smoker
volunteers in comparison with fifty of
apparently
healthy non-smoker volunteers as a control group. Information
for demographic study was taken from smokers and non smokers
subjects according to a questionnaire that included, name,
gender, age, consumption of pack number per day and duration of
smoking, in the period from the beginnings of March 2014 to the
end of June 2016. Through the molecular study, DNA was extracted
by using the genomic isolation kit, then subjected to PCR
analysis by using four sets of primers, then the PCR product
were sequenced to detect the TP53 mutations.
Results: The results of
the demographic study revealed that the highest number of
smokers located in the age group (36-45) represented 38 (25.33%)
of the total number with significant difference (P≤ 0.05). The
males constituted 91(60.67%) more than females 59 (39.33%) with
the high significant (P≤ 0.01). The distribution of smokers
according to pack consumption number by smokers a day showed
that the highest number 134 (89.33%) consumed more than one pack
per day against 16 (10.67%) of one pack a day with a high
significant (P≤ 0.01). Moreover
the highest
number 46
(30.67%)
had been smoking for
(16-20) year, while the lowest number
22 (14.67%)
of smokers had been smoking for
(5-10)
years with a high significant (P≤
0.01). The results of genetic study showed the
presence of many variations in
different locations
in TP53
gene such as G to C
polymorphism which were found in exon 5 with the percentage of
(47.3 %) among smokers in comparison with non smokers control
(0.0%). On the other hand, it was observed that exon 6 had
deletion in a high frequency among smoker individuals at a
percentage of (19.3%) rather than in the non-smokers (0.0%);
however, no genetic
variations were shown in
exons 7 and 8.
[Mohammed B, AL-Thwani A,
Kannan R. Demographic
and genetic study for a sample of Iraqi smokers.. Cancer Biology 2016;6(4):16-27].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
3.
doi:10.7537/marscbj060416.03.
Keywords:
demographic; genetic; Iraqi smokers |
Full Text |
3
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4
|
Post-renal
transplantation lymphoproliferative disorders: a retrospective
review of two cases
Najla
Moqadum,
SamiaSobki,
Najla Besharah, Amira Shaker
Department
of Central Military Laboratory and Blood Bank, Prince Sultan
Military Medical City, Riyadh, Saudi Arabia.
Najlatm2011@hotmail.com
Abstract: Background:
Post-transplant lymphoproliferative disorders (PTLD) encompass a
heterogeneous spectrum of conditions ranging from reactive
plasmacytic hyperplasia to malignant lymphoma. Many PTLD cases
are a result of infection with Epstein–Barr virus (EBV). EBV is
frequently detected in PTLD cells, and PTLD risk is highest
among children and recipients who are EBV seronegative at the
time of transplantation. PTLD is identified by having a high
index of suspicion in the appropriate clinical setting. The
diagnosis is made by histopathological evidence of
lymphoproliferation, commonly with the presence of EBV DNA, RNA,
or protein detected in tissue. Diagnosis of PTLD is not always
straightforward. Despite of improvements with new tolerable
therapies, survival of PTLD patients remains inferior,
necessitating further international cooperation to improving
long-term outcome of PTLD patients. We report here 2 cases of
monomorphic B-cell PTLD (multiple myeloma and burkitt lymphoma)
after successful renal transplantation.
We compare clinicopathological features of these 2 cases with
few cases reported in literature.
[Najla
Moqadum, Samia Sobki, Najla Besharah, Amira Shaker.
Post-renal transplantation lymphoproliferative
disorders: a retrospective review of two cases.
Cancer Biology
2016;6(4):28-31].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
4. doi:10.7537/marscbj060416.04.
Keywords:
Renal transplant, PTLD, Multiple myeloma, Burkitt lymphoma |
Full Text |
4
|
5
|
Induction Chemotherapy With
Capecitabine And Oxaliplatin (CAPOX) Followed By Concomitant
Chemoradiotherapy Before Surgical Resection In Patients With
Locally Advanced Rectal Cancer
Mohamed El-Shebiney M.D. and Alaa
Maria M.D.
Clinical Oncology Department,
Faculty of Medicine, Tanta University Hospital, Egypt.
alaamaria1@hotmail.com
Abstract: Background:
Concomitant
chemoradiotherapy (CRT) followed by total mesorectal excision
(TME) is standard treatment for locally advanced rectal cancer.
Induction chemotherapy has the advantage of earlier
administration of systemic therapy and may improve distant
control. Purpose:
The purpose of the
current study was to assess the efficacy and toxicity
of induction chemotherapy
(CAPOX) followed by
concomitant CRT before
surgery in patients with locally advanced rectal cancer.
Patients and Methods:
A total of 31 patients
with locally advanced rectal cancer were randomly assigned to
induction CAPOX followed by
concomitant
capecitabine-RT and surgery, then
the patients were received an
additional 4 cycles adjuvant capecitabine.
The primary end point was
assessment of pathological complete response (pCR) and the
feasibility of surgical resection with sphincter preservation.
Results:
All patients underwent surgery
with sphincter preservation procedure represented in
64.5%
of patients. Complete resection (R0) was recorded in 93.5%, T
downstaging in 61.3%
and N downstaging in 51.6%. Pathological complete response was
recorded in 19.4%.
Two-year OS and DFS rates were 83%
and 67.4%, respectively. Diarrhea was the most common grade 3/4
toxicity seen during the induction and
concomitant
CRT phases.
Conclusions:
Our results demonstrated
that, induction CAPOX followed by capecitabine-RT is feasible
with tolerable toxicity and results in encouragingly high rates
of pCR, R0 resection, sphincter preservation and tumor
downstaging in patients with locally advanced rectal cancer.
Additional studies of this approach to examine more optimal
regimens are warranted.
[Mohamed
El-Shebiney and Alaa Maria.
Induction Chemotherapy With Capecitabine And Oxaliplatin (CAPOX)
Followed By Concomitant Chemoradiotherapy Before Surgical
Resection In Patients With Locally Advanced Rectal Cancer. Cancer Biology 2016;6(4):32-40].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
5.
doi:10.7537/marscbj060416.05.
KeyWords:
Rectal cancer, induction chemotherapy, combined
chemoradiotherapy, sphincter preservation |
Full Text |
5
|
6
|
Integration of
Neoadjuvant Chemotherapy and Interval Debulking Surgeries in
Patients with Advanced Epithelial Ovarian Cancer: Our
Experience.
Loaie El-Helw1,2, Abeda Raiyan2, Hanaa
Elkhenini3,4,
Rajanee Bhana2
1The
department of medical oncology, Mansoura University, Egypt,
2 The Royal Stoke Hospital, Stoke-on-Trent, UK, 3The
department of public health, Mansoura University, Egypt, 4The
department of E-Health, the University of Manchester, UK
loaieelhelw@hotmail.com,
loaie.elhelw@uhns.nhs.uk
Abstract:
Purpose:
Neoadjuvant chemotherapy (NAC) and interval debulking surgery
(IDS) after 3 NAC cycles is an acceptable approach to achieve
optimal cytoreduction in patients with advanced epithelial
ovarian cancer (AEOC) who are not candidate for primary
debulking surgery (PDS). The best timing of cytoreductive
surgery and the role of late debulking surgery (LDS) after 6
cycles of NAC are still unclear. We aimed to study the outcome
of such patients who were treated in our centre during the last
5 years.
Methods:
This was a retrospective study of AEOC patients who had NAC with
or without IDS/LDS in the Royal Stoke Hospital, Stoke-On-Trent
between July 2009 and July 2014.
Results:
One hundred and eight patients with AEOC were treated under our
oncology team during that period. Sixty six patients (61.1%)
were in stages III and 42 (38.9%) in stage IV. All patients
received NAC; 64 patients (59.3%) had paclitaxel and carboplatin
regimen and 44 (40.7%) single agent carboplatin. Response to
chemotherapy was assessed after 2 cycles; 81 patients (75%) had
partial response, 21 (19.4%) stable disease and 6 (5.6%)
progressive disease. Forty one patients (38%) proceeded to IDS
after cycle 3 and 11 patients (10.2%) to LDS after cycle 6 but
56 (51.9%) had no debulking surgery (NDS).
After a median follow
up period of 18 months (6-84 months), 95 patients (88%) had
relapsing/progressive disease. The median PFS durations were 13
and 12 months for patients who had either IDS and LDS
respectively compared to 8 months for NDS. The 2 years PFS
probabilities were 18% for patients who had IDS, 15% for LDS
compared to 0% for NDS (P 0.000 Log rank test). The median
overall survival (OS) durations were 48, 33 and 18 months for
patients who had IDS, LDS and NDS respectively. The 2 years OS
probabilities were 75% for patients who had either IDS, or LDS
compared to 38% for NDS (P.000 Log rank test). Conclusion:
In our study, we documented PFS and OS advantages for
patients who IDS or LDS compared to NDS and therefore should be
considered whenever possible as part of the primary treatment of
AEOC patients. Interval debulking surgery (IDS) offers longer
duration and higher probabilities of PFS and OS compared to LDS.
More patients-therefore- should be selected for IDS. There is a
need for improving NAC possibly with integrating target agents
and the use of more intensified schedules. ICON8B trial is
currently addressing that.
[Loaie
El-Helw, Abeda Raiyan, Hanaa Elkhenini,
Rajanee Bhana. Integration of Neoadjuvant Chemotherapy and Interval Debulking
Surgeries in Patients with Advanced Epithelial Ovarian Cancer:
Our Experience.
Cancer Biology
2016;6(4):41-47].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
6. doi:10.7537/marscbj060416.06.
Key words:
advanced ovarian cancer-neoadjuvant chemotherapy-surgical
debulking |
Full Text |
6
|
7
|
CRISPR and
Cancer Biology Research
Literatures
Ma Hongbao *, Margaret Young **,
Zhu Yucui ***, Yang Yan *, Zhu Huaijie ****
* Brookdale University Hospital
and Medical Center, Brooklyn, New York 11212, USA,
ma8080@gmail.com;
** Cambridge, MA 02138, USA; *** Department of Dermatology,
Columbia University Medical Center, 630 West, 168th Street, New
York, New York 10032, USA; **** The 2nd Affiliated Hospital of
Zhengzhou University, 2 Jingba Road, Zhengzhou,
Henan 450014, China.
jacksun689@gmail.com,
yz81@columbia.edu; 011-86-150-3711-5732
Abstract:
Cancer is the general name for a
group of more than 100 diseases. Although there are many kinds
of cancer, all cancers start because abnormal cells grow out of
control. Untreated cancers can cause serious illness and death.
The body is made up of trillions of living cells. Normal body
cells grow, divide, and die in an orderly fashion. During the
early years of a person’s life, normal cells divide faster to
allow the person to grow. After the person becomes an adult,
most cells divide only to replace worn-out or dying cells or to
repair injuries.
Clustered
regularly interspaced short palindromic repeats (CRISPR) are
segments of prokaryotic DNA
containing
short, repetitive base sequences. Each repetition is followed by
short segments of spacer DNA
from previous exposures to foreign DNA. Small clusters of cas (CRISPR-associated
system) genes are located next to CRISPR sequences.
CRISPR-Cas9 is a new powerful
technique for the gene editing target. This article introduces
recent research reports as references in the related studies.
[Ma H, Young M, Zhu Y, Yang Y,
Zhu H. CRISPR and
Cancer Biology Research
Literatures.
Cancer Biology
2016;6(4):48-108].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
7. doi:10.7537/marscbj060416.07.
Key words:
cancer; life; research; literature; cell; CRISPR; Cas9 |
Full Text |
7
|
8
|
Quantum and
Cancer Biology Research
Literatures
Ma Hongbao *, Margaret Young **,
Zhu Yucui ***, Yang Yan *, Zhu Huaijie ****
* Brookdale University Hospital
and Medical Center, Brooklyn, New York 11212, USA,
ma8080@gmail.com;
** Cambridge, MA 02138, USA; *** Department of Dermatology,
Columbia University Medical Center, 630 West, 168th Street, New
York, New York 10032, USA; **** The 2nd Affiliated Hospital of
Zhengzhou University, 2 Jingba Road, Zhengzhou,
Henan 450014,
China.
jacksun689@gmail.com,
yz81@columbia.edu; 011-86-150-3711-5732
Abstract:
Cancer is the general name for a
group of more than 100 diseases. Although there are many kinds
of cancer, all cancers start because abnormal cells grow out of
control. Untreated cancers can cause serious illness and death.
The body is made up of trillions of living cells. Normal body
cells grow, divide, and die in an orderly fashion. During the
early years of a person’s life, normal cells divide faster to
allow the person to grow. After the person becomes an adult,
most cells divide only to replace worn-out or dying cells or to
repair injuries.
Quantum theory has a significant relationship to the cancer
biology.
This article introduces recent research reports as references in
the related studies.
[Ma H, Young M, Zhu Y, Yang Y,
Zhu H. CRISPR and
Cancer Biology Research
Literatures.
Cancer Biology
2016;6(4):109-174].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
8.
doi:10.7537/marscbj060416.08.
Key words:
cancer; life; research; literature; cell; CRISPR; Cas9 |
Full Text |
8
|
9
|
To Assessment
on Prospective and Confront of Nanomachines – A Conceptual View
Anandan K1, Dr Suresh Prabhu P2
1.
Research Scholar, Department of Mechanical Engineering, Anna
University Chennai, Tamilnadu, India
2.
Director, Mechanical Sciences, United Institute of Technology,
Coimbatore, India
E mail:
researchsureshprabhu@gmail.com
Abstract:
Nanomachines are devices built from individual atoms. Some
researchers believe that nanomachines will one day be able to
enter living cells to fight disease. They also hope to one day
build nanomachines that will be able to rearrange atoms in order
to construct new objects. If they succeed, nanomachines could be
used to literally turn dirt into food and perhaps eliminate
poverty. In this article we’ll outline some of the possible uses
of nanomachines. I will then assess some of the problems
involved in producing such machines. One of the problems we’ll
look at is that of producing self-replicating machines. In this
manuscript conclusion will be that nanomachines offer humanity
hope for the future, so the research should be pursued. However,
I will also suggest that the dangers involved in producing self
replicating machines outweigh the potential gains and for this
reason, self-replicating machines should not be built.
[Anandan
K, Suresh Prabhu P. To
Assessment on Prospective and Confront of Nanomachines – A
Conceptual View.
Cancer Biology
2016;6(4):175-179].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
9. doi:10.7537/marscbj060416.09.
Keyword:
Nanomachines,
Nanotechnology, Challenges and Opportunities |
Full Text |
9
|
10
|
To Examination on
Optimum Utilisation of Kinetic Energy
and Operational Features from Tidal Stream Turbine
Madan D1, Dr Rajendran M2
1.
Research Scholar,
Department of Mechanical Engineering, Anna University Chennai,
Tamilnadu, India
2.
Professor and Head,
Department of Mechanical Engineering, Government College of
Technology, Coimbatore, Tamilnadu, India.
Email:
madan.research@gmail.com
Abstract:
Tidal stream energy represents a large resource along the power
inflow of a current follows a cubic law and the tidal stream
energy is only attractive where the current exceeds 2m/s during
a sufficient time along the year. Some examples of the
theoretical resource are shown for different sites and tide
amplitude. The tidal stream velocity varies along the day and
the month. The theoretical output is discussed for a typical
site in terms of instantaneous power and annual production. For
a given site and rotor diameter, economical factors invite to
limit the electrical capacity to an economical optimum. The main
features of the Marenergie type of tidal stream turbine are
presented. The design has been governed by the following
considerations: (a) This source of renewable energy must have an
acceptable cost, so the overall concept must be economically
viable (b) The tidal turbine must work in a submarine
environment where maintenance is very difficult and the
machinery must be made as simple as possible (c) All marine
operations for installation and maintenance must take into
account the strong currents prevailing in the potential sites
(d) A compromise must be found between the capital cost and the
yearly energy production and (e) The interaction of the waves
with the current must be considered.
[Madan
D, Rajendran M.
To Examination on Optimum
Utilisation of Kinetic Energy and Operational Features from
Tidal Stream Turbine.
Cancer Biology
2016;6(4):180-184].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
10. doi:10.7537/marscbj060416.10.
Keywords:
Tidal, turbines, stream, current, rotor and wave |
Full Text |
10
|
11
|
A comparison between Curie
temperature of nano and bulk Al doped nickel ferrite
O. RAHMANi
Department
of Physics, Faculty of
Science, Islamic Azad University, Takestan, Iran.
*omid_325@yahoo.com
Abstract: Nanocrystalline
Al-doped nickel ferrite NiAl0.5Fe1.5O4 has been synthesized by
sol-gel method. The X-ray diffraction (XRD) revealed that the
powder obtained is single phase with spinel structure. Average
crystallite size has been calculated by Scherrer's formula.
Magnetic hysteresis loop was measured at room temperature with a
maximum applied field of 8000 Oe. The Curie temperature (Tc)
obtained by Faraday balance. The results show that magnetization
decreases whit decreasing of particle size and Curie temperature
increases.
[Kharkwal G, Mehrotra
P, Rawat YS. A comparison between Curie temperature of nano
and bulk Al doped nickel ferrite. Cancer Biology 2016;6(4):185-187].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
11. doi:10.7537/marscbj060416.11.
Keywords:
Sol-gel; Ni-Al ferrite;
Nanocrystalline; Magnetic properties; Curie temperature. |
Full Text |
11
|
12 |
Angiogenesis in astrocytomas:
An immunohistochemical study of VEGF, factor VIII, and COX-2
expression
Omnia MK Rizk1, Eman
M. Saied2, Dalia ES Abd El-Maqusod3
1Pathology
Department, Faculty of Medicine, Tanta University, Egypt
2Pathology
Department - Faculty of Medicine - Kafrelsheikh University,
Egypt
3El-Menshawy
General Hospital, Egypt
omnia_kamelrizk@outlook.com
Abstract: Background & aim:
Astrocytomas are
histologically classified into grades I through IV on the basis
of cellularity, nuclear atypia, mitotic activity,
pseudopalisading necrosis and/ or microvascular proliferation.
Angiogenesis plays an important role in the growth and
progression of asrtocytomas that exhibit marked and aberrant
blood vessel formation indicating angiogenic endothelial cells
as a potential target for tumor treatment.
Materials & methods: This work was designed to study the
role of angiogenesis in the growth and progression of
astrocytomas, by studying the immunohistochemical expression of
vascular endothelial growth factor (VEGF), factor VIII, and
Cyclooxygenase-2 (COX-2) on 78 retrospective cases of
astrocytoma. Results:
VEGF immunoreactivity was
detected 87.2% of the studied cases, while 82.1% of the studied
cases showed positive COX-2 expression. The expression of both
VEGF and COX-2 showed significant increase with increasing tumor
grade (p < 0.05). The relationship between the tumor grade and
microvascular density (MVD) increased significantly (p < 0.05).
A significant positive correlation was observed between the
immunoreactive scores of VEGF, COX-2, and MVD (p < 0.05).
Conclusion: The increase in VEGF expression and MVD in
astrocytomas indicates the significant role of angiogenesis in
their development and progression. The significant positive
association between VEGF expression, MVD, and COX-2 expression
suggests that COX-2 contributes to angiogenesis in astrocytomas
possibly by upregulation of VEGF.
[Omnia MK Rizk, Eman M. Saied,
Dalia ES Abd El-Maqusod Angiogenesis in astrocytomas: An
immunohistochemical study of VEGF, factor VIII, and COX-2
expression. Cancer Biology 2016;6(4):188-195].
ISSN: 2150-1041 (print); ISSN: 2150-105X (online).
http://www.cancerbio.net.
12. doi:10.7537/marscbj060416.12.
Keywords:
Astrocytoma, COX-2, VEGF, factor VIII |
Full Text |
12 |
The manuscripts in this
issue were presented as online first for peer-review starting
from
October 18, 2016.
All comments are
welcome:
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