[1]
Special Report: Fecal DNA Analysis for Colon Cancer Screening
[226,7 KB]
From [www.bcbs.com] Last viewed: 07.09.2006
Technology Evaluation Center
BlueCross
BlueShield
Association
®
®
An Association
of Independent
Blue Cross and
Blue Shield Plans
©2006 Blue Cross and Blue Shield Association. Reproduction without prior authorization is prohibited.
1
NOTICE OF PURPOSE: TEC Assessments are scientific opinions, provided solely for informational purposes. TEC Assessments
should not be construed to suggest that the Blue Cross Blue Shield Association, Kaiser Permanente Medical Care Program or the
TEC Program recommends, advocates, requires, encourages, or discourages any particular treatment, procedure, or service; any
particular course of treatment, procedure, or service; or the payment or non-payment of the technology or technologies evaluated.
Assessment
Program
Volume 21, No. 6
August 2006
Executive Summary
Background
Various methods for ...
[2]
Prolonged exposure of colon cancer cells to the epidermal growth ...
[583,0 KB]
From [www.wjgnet.com] Last viewed: 07.09.2006
COLORECTAL CANCER
Prolonged exposure of colon cancer cells to the epidermal
growth factor receptor inhibitor gefitinib (Iressa™) and to the
antiangiogenic agent ZD6474: Cytotoxic and biomolecular
effects
Amalia Azzariti, Letizia Porcelli, Jian-Ming Xu, Grazia Maria Simone, Angelo Paradiso
www.wjgnet.com
Amalia Azzariti, Letizia Porcelli, Grazia Maria Simone, Angelo
Paradiso, Clinical Experimental Oncology Laboratory, National
Cancer Institute, Bari, Italy
Jian-Ming Xu, Beijing 307 Hospital Cancer Center, Beijing
100039, China
Supported by grants from the Italian Association for Cancer
Research (AIRC-2004) and from the Italian Ministry of Health,
Project ex art.12, Region of Emilia Romagna RF02
Correspondence to: Angelo Paradiso, MD, Head Clinical
Experimental Oncology Laboratory, National Cancer Institute, Via
Amendola 209, 70125 Bari, Italy. a.p...
[3]
Readers Bring Attention to Value of Surgical Intervention in ...
[40,9 KB]
From [www.ons.org] Last viewed: 07.09.2006
C
LINICAL
J
OURNAL OF
O
NCOLOGY
N
URSING
• V
OLUME
5, N
UMBER
1 • L
ETTERS TO THE
E
DITOR
5
L
ISA
S
CHULMEISTER
, RN, MN, CS, OCN
®
E
DITOR
L
ETTERS TO THE
E
DITOR
Readers Bring Attention to
Value of Surgical Intervention
in Treating Colon Cancer
Some of the information provided in the
article “Therapeutic Options for Advanced
Colorectal Cancer ,” by Deborah T. Berg,
RN, BSN, and Christine Lilienfeld, RN,
BSN, OCN
®
( Clinical Journal of Oncology
Nursing, Vol. 4, pp. 209–216), is disputable.
Several points are not consistent with cur-
rent publications and the standard of care for
metastatic colon cancer ...
[4]
A Novel Biomarker for Diagnosis of Ulcerative Colitis and Colon ...
[74,5 KB]
From [www.umdnj.edu] Last viewed: 07.09.2006
A Novel Biomarker for Diagnosis of Ulcerative Colitis and Colon Cancer
Background
Tropomyosins are microfilament-associated proteins found in all eukaryotes and have been implicated
in autoimmune diseases such as ulcerative colitis. To date, eight different isoforms (hTM1, hTM2,
hTM3, hTMsma, hTM5a, hTM5b, hTM4, and hTM5) have been identified. Although anti-
tropomyosin autoantibodies have been detected in the sera of patients with ulcerative colitis, the
autoantigen triggering the autoantibody response has not been definitively identified. Previous studies
at UMDNJ have identified hTM5 as the predominant immunogen in ulcerative colitis patients.
Ulcerative colitis is difficult to diagnose because its symptoms are similar to other intestinal disorders.
Furthermore, about 5% of patients with ulcerative colitis develop colon cancer . Thus, the
identification of the autoantigen(s), in particular, the specific ...
[5]
A Comparison of Laparoscopically Assisted and Open Colectomy for ...
[111,9 KB]
From [medschool.umaryland.edu] Last viewed: 07.09.2006
original article
The
new england journal
of
medicine
n engl j med 350;20 www.nejm.org may 13, 2004
2050
A Comparison of Laparoscopically Assisted
and Open Colectomy for Colon Cancer
The Clinical Outcomes of Surgical Therapy Study Group*
The preparation of this article was over-
seen by the writing committee of the Clin-
ical Outcomes of Surgical Therapy Study
Group of the Laparoscopic Colectomy Trial
(Heidi Nelson, M.D., Daniel J. Sargent,
Ph.D., H. Sam Wieand, Ph.D., James Flesh-
man, M.D., Mehran Anvari, M.D., Steven
J. Stryker, M.D., Robert W. Beart, Jr., M.D.,
Michael Hellinger, M.D., Richard Flanagan,
Jr., M.D., Walter Peters, M.D., and David
Ota, M.D.), who assume responsibility for
the overall content and integrity of the arti-
cle. Address reprint requests to Dr. Heidi
Nelson at the Division of Colon and Rectal ...
[6]
Corporate Medical Policy Colon Cancer Screening
[61,7 KB]
From [www.bcbsnc.com] Last viewed: 07.09.2006
Corporate Medical Policy
Colon Cancer Screening
File Name:
colon_cancer_screening
Policy Number:
SUR6164
Origination:
12/2000
Last Review:
4/2006
Next Review:
4/2008
Description of Procedure or Service
When colorectal cancer is diagnosed at an early, localized state, five-year survival is 90%, yet only 37% of
incident cases are diagnosed while still localized. The same methods used to detect colorectal cancers at
early, curable stages can also identify and remove adenomas, which give rise to colorectal cancer . Methods
for early detection can therefore actually prevent colorectal cancer .
Definitions of Early Detection Methods are as follows:
?
Fecal Occult Blood Test (FOBT) - FOBT is a laboratory procedure that refers to the implementa-
tion of the protocol for collecting and testing six samples from three consecutive stools at home. ...
[7]
Colon Cancer Patients Who Stop Chemotherapy Double Death Rate
[243,6 KB]
From [www.mailman.hs.columbia.edu] Last viewed: 07.09.2006
Colon Cancer Patients Who Stop Chemotherapy Double Death Rate
New research indicates that as many as 30 percent of patients with stage III colon cancer
who were prescribed six months of chemotherapy with a combination of 5-fluorouracil
and leucovorin stopped their treatment prematurely. Stopping chemotherapy for colon
cancer was shown to be equivalent to receiving no treatment at all. The findings add to
the arsenal of reasons why colon cancer patients, and all cancer patients, need to
complete their chemotherapy regimens whenever possible.
Previous studies have shown that not completing chemotherapy regimens for breast
cancer is associated with shorter survival. This is the first study to look at a link between
mortality rates from colon cancer and treatment adherence.
"The intuitive thinking is that if you complete most of a treatment regimen, you should
get most of the treatment benefit," ...
[8]
Unexplained Inversion of the Incidence Ratio of Colon and Rectal ...
[21,4 KB]
From [www.gmds2006.de] Last viewed: 07.09.2006
Unexplained Inversion of the Incidence Ratio of Colon and Rectal Cancer among Men in East Germany
Stang A
1
, Stabenow R
2
, Stegmaier C
3
, Eisinger B
2
, Bischoff-Hammes E
1,4
, Jöckel KH
4
1
Institute of Medical Epidemiology, Biometry and Informatics, Medical Faculty, Martin-Luther-University of Halle-Wittenberg, Magdeburger Str. 27, 06097 Halle,
Germany
2
Common Cancer Registry of Berlin, Brandenburg, Mecklenburg-Vorpommern, Sachsen-Anhalt, and the Free States of Sachsen and Thüringen (GKR), Brodauer Str.
16-22, 12621 Berlin, Germany
3
Saarland Cancer Registry, Virchowstr. 7, 66119 Saarbrücken, Germany
4
Institute of Medical Informatics, Biometry and Epidemiology, University Hospital, University of Duisburg-Essen, Hufelandstr. 55, 45147 Essen, Germany ...
[9]
colon cancer fact sheet
[50,2 KB]
From [www.tbdhu.com] Last viewed: 07.09.2006
Cancer :
Cancer is a common disease and is
identified in 1 out of 3 Canadians
in their lifetime. It begins as a
change in a single cell and this cell
multiplies and creates a small group
of abnormal cells within a specific
tissue. This uncontrolled growth
can lead to the development of a
tumour. The development of cancer
is due to both genetic and non-
genetic factors.
Colon cancer is one of the more
frequently seen types of cancers and
is diagnosed in approximately
16,000 people in Canada every
year. Most individuals who have
colon cancer have not inherited a
gene that has predisposed them to
cancer . Their cancer is thought to
occur by chance and the cause is
unknown. It is estimated that only
5-10% of colon cancers are
hereditary and said to “run in
families”.
Colorectal Cancer
Cancer Genetics:
Genes ...
[10]
Corporate Medical Policy Genetic Testing for Colon Cancer
[89,6 KB]
From [www.bcbsnc.com] Last viewed: 07.09.2006
Corporate Medical Policy
Genetic Testing for Colon Cancer
File Name:
genetic_testing_for_colon_cancer
Policy Number:
MED1171
Origination:
5/2004
Last Review:
4/2006
Next Review:
4/2008
Description of Procedure or Service
There are currently two well-defined types of hereditary colorectal cancer , familial polyposis (FAP) and
hereditary non polyposis colorectal cancer (HNPCC). FAP is typically apparent by age 10. If left untreated,
all affected individuals will go on to develop colorectal cancer . FAP accounts for 1% of colorectal cancer
and may also be associated with osteomas of the jaw, skull, and limbs; sebaceous cysts; and pigmented spots
on the retina, referred to as Gardner’s syndrome. Individuals with HNPCC tend to have early-onset colorec-
tal cancer , right-sided tumors, and often multiple cancers. ...
[11]
Colon Cancer
[291,3 KB]
From [www1.va.gov] Last viewed: 07.09.2006
What is colon cancer ?
It is the growth of harmful cells in the rectum or
large intestine ( colon ).
What is a polyp?
?
A polyp is a bump on the lining of the
colon or rectum
?
Left in place, some polyps may become a
larger lump or cancer
?
Colon cancer almost always starts with a
polyp
?
Early removal of a polyp stops the cancer
before it starts (for both men and women)
What are the signs of colon
cancer ?
?
Early screening is very important. There
are usually no symptoms at first
?
The number of cases of colon cancer rises
greatly from age 50 to 70
Later you may have:
?
Bloody or black, tarry stools
?
Cramps or a full feeling
?
A change in bowel habits
?
Weight loss for no reason
?
...
[12]
Colon Cancer Alliances 2nd Annual Colorectal Cancer Conference
[63,0 KB]
From [www.ccalliance.org] Last viewed: 07.09.2006
6
th
Annual National Colorectal Cancer Conference
Finding HOPE: Healing, Options, Peer Support, Education
September 15-17, 2006
Just outside of Chicago in Oak Brook, Illinois
Richard Farrell Memorial Scholarship Fund Application
Scholarship Guidelines:
CCA is committed to making this event accessible to as many survivors, caregivers and
advocates as possible based on the funding available. We will make every effort to assist all
applicants based on their needs. The following guidelines apply:
Scholarships will be limited to survivors, caregivers, CCA volunteers and those playing
an integral role in the colorectal cancer community.
Scholarships may apply to conference registration fee, travel and/or lodging expenses.
No more than one scholarship will be awarded to an individual in any given year.
All scholarship decisions are final. There is no appeal ...
[13]
Follow-up Regimens for Colon and Rectal Cancer
[54,1 KB]
From [www.facs.org] Last viewed: 07.09.2006
Follow-up Regimen for Colon and
Rectal Cancer
Dennis L. Rousseau Jr. M.D./Ph.D., FACS
Assistant Professor of Surgery
Division of Surgical Oncology
University of Texas Health Science Center
San Antonio
Page 2
Colorectal Cancer
• 149,000 cases estimated for 2006
– 3
rd
most common cancer of men and women
• 55,200 deaths in 2006
– 2
nd
most common cause of cancer death in
men
– 3
rd
most common cause of cancer death in
women
• Lifetime incidence in US
– Men – 1 in 17
– Women – 1 in 18
Jemal et al. CA Cancer J Clin 2006;56:106-130
Page 3
Colorectal Cancer
• 65 – 70% cases treated with curative resection
• 100,000 patients per year in need of follow-up
• Stage I patients
– 10-15% of cases
– >90% 5-year ...
[14]
Differential Expression in SAGE: Normal vs. Primary Colon Cancer
[52,2 KB]
From [www.stat.ohio-state.edu] Last viewed: 07.09.2006
of the file http://www.stat.ohio-state.edu/~sabrina/presentation/bio882.ppt . G o o g l e automatically generates html versions of documents as we crawl the web. To link to or bookmark this page, use the following url: http://www.google.com/search?q=cache:JpaQJM0eOuUJ:www.stat.ohio-state.edu/~sabrina/presentation/bio882.ppt+colon+cancer+filetype:pdf+OR+filetype:doc+OR+filetype:ppt+OR+filetype:xls+OR+filetype:rtf&hl=it&ct=clnk&cd=334&lr=lang_en
Google is neither affiliated with the authors of this page nor responsible for its content.
These search terms have been highlighted:
colon
cancer
1581
Differential Expression in SAGE: Normal vs. Primary Colon Cancer
Shuyan Wan
Method
Modified t-test (Baggerly 2003)
Bayesian model based t-test (Vencio 2004)
Both account for within-group biological variability and deal ...
[15]
Image Analysis of Extracellular Matrix Topography of Colon Cancer ...
[541,3 KB]
From [www.microscopy-analysis.com] Last viewed: 07.09.2006
BIOGRAPHY
Dr Sarah Glover received
her medical degree from
Midwestern University in
1998 and completed
training in internal medi-
cine and gastroenterol-
ogy at the University of
Illinois at Chicago. Her current research
focus is on the role of the extracellular
matrix topography in post neoplastic trans-
formation and metastasis in colon cancer .
ABSTRACT
Scanning electron microscope stereoscopy
(SEM-S) has been used for many years to
characterize 3D features of non-biological
andbiological specimens. Traditionally, data
production by SEM-S required tedious man-
ual measurements. Digital image processing
has led to the development of software for
mathematically characterizing 3D surfaces.
These programs greatly simplify SEM-S and
provide details about features of a specimen
including its area, volume, and roughness.
We report the use of ...
[16]
Recommendations for Colon Cancer Screening Questioned
[100,9 KB]
From [www.stfm.org] Last viewed: 07.09.2006
465
Vol. 38, No. 7
Letters to the Editor
3. Starr S, Ferguson WJ, Haley HL, Quirk M.
Community preceptors’views of their identi-
ties as teachers. Acad Med 2003;78:820-5.
4. Bickel J, Brown AJ. Generation X: implica-
tions for faculty recruitment and develop-
ment in academic health centers. Acad Med
2005;80:205-10.
Note: Further references are available from the
authors of this letter.
Recommendations for
Colon Cancer Screening
Questioned
To The Editor:
Recently, I read that in July 2005,
the legal opinion of the American
College of Gastroenterology (ACG)
concluded that there is “‘potential
litigation exposure’ inherent in
credentialing physicians who lack
board certification in gastroenterol-
ogy or eligibility for such certifica-
tion.”
1
“Turf wars” between family
physicians and other subspecialties ...
[17]
Genetic Screening Model Identifies Colon Cancer Risk
[20,0 KB]
From [www.pac3.org] Last viewed: 07.09.2006
Genetic Screening Model Identifies Colon Cancer Risk
06.28.06, 12:00 AM ET
WEDNESDAY, June 28 (HealthDay News) -- Scottish researchers say they've developed a method that
can better identify people at risk of certain types of hereditary colon cancer , as well as help guide
treatment choices for those already diagnosed with colon cancer .
In a study in the June 29 issue of the New England Journal of Medicine , the University of Edinburgh
researchers detailed the two-stage screening model they developed to genetically identify those with
hereditary cancers and the results of the study used to validate their model.
"The method [we developed] allows rapid assessment of predicted likelihood that any given patient newly
diagnosed with bowel cancer has a mutation," said one of the study's authors, Dr. Malcolm G. Dunlop, a
professor of coloproctology and head of the Colon Cancer Genetics Group at Western ...
[18]
NP Poster 138 Colon Cancer Screening: knowledge, Attitudes, and ...
[63,1 KB]
From [www.aanp.org] Last viewed: 07.09.2006
NP Poster 138
Colon Cancer Screening: knowledge, Attitudes, and Behavior Among African-
American Women
Jennifer Swedmark, ARNP MSN, Tallahassee, FL (email directed to
dfrank@nursing.fsu.edu ); D. Frank, ARNP, PhD, Professor, Florida Sate University (FSU)
Tallahassee, FL, L Grubbs, ARNP PhD, FSU
PURPOSE: The purpose of this research was to investigate the frequency of colorectal cancer
screening African-American women aged 50 and older who are in the high risk category for
developing colorectal cancer and polyps. Additionally, their beliefs and attitudes were examined
through the guidance of the Health Belief Model to aid in the prediction of screening utilization.
METHODOLOGY: This randomized study used a descriptive/correlative, non-experimental
survey approach. Participants were recruited through faith-based organizations in 4 quadrants of a
north Florida city and were mailed the ...
[19]
Colon cancer in England_TrendsCover.psd
[232,2 KB]
From [www.uhce.ox.ac.uk] Last viewed: 07.09.2006
Page 2
Mortality trends in England; ICD9 (153), ICD10 (C18); File: Sepho 96-04 V2
Colon cancer in England 1996 to 2004.
Mortality trends
Authors: Michael Goldacre, Marie Duncan, Paula Cook-Mozaffari,
Matthew Davidson, Henry McGuiness, Daniel Meddings
Published by: Unit of Health-Care Epidemiology, Oxford University, and
South-East England Public Health Observatory, 2006
This document provides a profile of trends in mortality for colon cancer in
England. The period covered is January 1 1996 to December 31 2004. The
data are analysed from mortality files supplied to the South East England
Public Health Observatories (SEPHO) by the Office for National Statistics
(ONS). Mortality rates were calculated for the condition certified as the
underlying cause of death and for the disease certified as any mention on the
death certificates. Age-specific ...
[20]
ZNF306, a novel zinc finger transcription factor, drives colon ...
[72,8 KB]
From [www.biochemistry.org] Last viewed: 07.09.2006
0419
ZNF306, a novel zinc finger transcription factor, drives colon
cancer progression
Lin Yang, Stanley Hamilton, Lee Ellis, Gabriel Lopez-Bernstein,
Angela Sanguino, Douglas Boyd
MD Anderson Cancer Center, Houston, Texas, USA
In colon cancer , simultaneous mutation of the APC , p53 and K- Ras genes
is rare suggesting alternate genetic pathways. UniGene cluster analysis
identified an EST, corresponding to a novel zinc finger protein (ZNF306)
over-represented in colon cancer . RT-PCR confirmed elevated ZNF306
mRNA levels in 7/9 resected tumors. Stable ZNF 306 cDNA expression
in HCT 116 colon cancer cells (wild type p53/APC), increased soft agar
colony formation and 5FU-resistance. In vivo , ZNF306-overexpressing
HCT 116 cells yielded larger tumors than control cells (100 and 20 %
incidence respectively). Transduction of HT29 colon cancer cells with a
ZNF306 ...
[21]
Nebraska Colon Cancer Screening Program
[187,4 KB]
From [www.hhs.state.ne.us] Last viewed: 07.09.2006
Nebraska Health and Human Services
Nebraska Colon Cancer Screening Program
301 Centennial Mall South - P.O. Box 94817
Lincoln, NE 68509-4817
Toll Free: 1-800-532-2227
Fax: 471-0913
E-mail: ncp@hhss.ne.gov
Website: www.hhss.ne.gov/crc
CLIENT INFORMATION BOOKLET
In this booklet you will find information on how
Nebraska Colon Cancer Screening Program can serve you.
Fecal Occult
Blood T
est
Kit
Colonoscopy
Colon
Health
Screening
Exams
Version June 2006
Nebraska Colon Cancer Screening Program
Page 2
What is the Nebraska Colon Cancer Screening
Program (NCP)?
NCP is the newest program added to Every Woman Matters (EWM). Nebraska is one of only
five such programs in the nation. The goal of NCP is to increase screening for colon ...
[22]
Blood Test Shows Promise in Early Identification of Colon Cancer
[151,8 KB]
From [www.hhmi.org] Last viewed: 07.09.2006
0419
ZNF306, a novel zinc finger transcription factor, drives colon
cancer progression
Lin Yang, Stanley Hamilton, Lee Ellis, Gabriel Lopez-Bernstein,
Angela Sanguino, Douglas Boyd
MD Anderson Cancer Center, Houston, Texas, USA
In colon cancer , simultaneous mutation of the APC , p53 and K- Ras genes
is rare suggesting alternate genetic pathways. UniGene cluster analysis
identified an EST, corresponding to a novel zinc finger protein (ZNF306)
over-represented in colon cancer . RT-PCR confirmed elevated ZNF306
mRNA levels in 7/9 resected tumors. Stable ZNF 306 cDNA expression
in HCT 116 colon cancer cells (wild type p53/APC), increased soft agar
colony formation and 5FU-resistance. In vivo , ZNF306-overexpressing
HCT 116 cells yielded larger tumors than control cells (100 and 20 %
incidence respectively). Transduction of HT29 colon cancer cells with a
ZNF306 ...
[23]
A203( ? )- Colon cancer tissues_liver metastasis Specifications ...
[482,4 KB]
From [search.cosmobio.co.jp] Last viewed: 07.09.2006
For research use only
A203( ? )- Colon cancer tissues_liver metastasis
(formalin fixed)
Specifications:
• No. of cases: 18
• Tissue type: Colon cancer tissues_liver metastasis with
corresponding colon normal tissues
• No. of spots: 4 spots from each cancer case (72 spots)
18 non-neoplastic spots (18 spots)
•Total spots: 90
• Corresponding normal tissues with cancers: Yes
• Diameter: 1. 0 mm
Documents :
• Product specification: layout, summary of tissue spots
• H&E stained images
• Detailed pathological information
Layout:
1
2
3
4
5
6
7
8
9
10
A
B
C
D
E
F
G
H
I
:
colon , non malignant
:
colon , tumor
:
liver, metastatic tumor
:
one patient case
Page 2 ...
[24]
A203( ? ): Colon cancer tissues_liver metastasis Specifications ...
[482,1 KB]
From [search.cosmobio.co.jp] Last viewed: 07.09.2006
For research use only
A203( ? ): Colon cancer tissues_liver metastasis
(formalin fixed)
Specifications:
• No. of cases: 18
• Tissue type: Colon cancer tissues_liver metastasis with
corresponding colon normal tissues
• No. of spots: 4 spots from each cancer case (72 spots)
18 non-neoplastic spots (18 spots)
•Total spots: 90
• Corresponding normal tissues with cancers: Yes
• Diameter: 1. 0 mm
Documents :
• Product specification: layout, summary of tissue spots
• H&E stained images
• Detailed pathological information
Layout:
1
2
3
4
5
6
7
8
9
10
A
B
C
D
E
F
G
H
I
:
colon , non malignant
:
colon , tumor
:
liver, metastatic tumor
:
one patient case
A1
...
[25]
A203( ? )- Colon cancer tissues_liver metastasis Specifications ...
[482,1 KB]
From [search.cosmobio.co.jp] Last viewed: 07.09.2006
For research use only
A203( ? )- Colon cancer tissues_liver metastasis
(formalin fixed)
Specifications:
• No. of cases: 14
• Tissue type: Colon cancer tissues_liver metastasis with
corresponding normal tissues
• No. of spots: 4 spots from each cancer case (56 spots)
14 non-neoplastic spots (14 spots)
•Total spots: 70
• Corresponding normal tissues with cancers: Yes
• Diameter: 1. 5 mm
Documents :
• Product specification: layout, summary of tissue spots
• H&E stained images
• Detailed pathological information
Layout:
1
2
3
4
5
6
7
8
9
10
A
B
C
D
E
F
G
:
colon , non malignant
:
colon , tumor
:
liver, metastatic tumor
:
one patient case
Page 2
Summary ...
[26]
A713( ? ):Test slide-Colon cancer tissues _liver metastasis ...
[246,2 KB]
From [search.cosmobio.co.jp] Last viewed: 07.09.2006
For research use only
A713( ? ):Test slide- Colon cancer tissues
_liver metastasis
(formalin fixed)
Specifications:
• No. of cases: 4
• Tissue type: Colon cancer tissues_liver metastasis with
corresponding normal tissues
• No. of spots: 4 spots from each cancer case (16 spots)
4 non-neoplastic spots (4 spots)
•Total spots: 20
• Corresponding normal tissues with cancers: Yes
• Diameter: 1. 5 mm
Documents :
• Product specification: layout, summary of tissue spots
• H&E stained images
• Detailed pathological information
Layout:
1
2
3
4
5
A
B
C
D
:
colon , non malignant
:
colon , tumor
:
liver, metastatic tumor
:
one patient case
Page 2
Summary of tissue spots
For research use ...
[27]
A203 ? -Colon cancer tissues Specifications: • No. of cases: 45 ...
[578,0 KB]
From [search.cosmobio.co.jp] Last viewed: 07.09.2006
For research use only
A203 ? - Colon cancer tissues
(formalin fixed)
Specifications:
• No. of cases: 45
• Tissue type: Colon cancer tissues
• No. of spots: 2 spots from each tumor case (90 spots)
8 non-neoplastic spots (8 spots)
•Total spots: 98
• Corresponding normal tissues with cancers: No
• Diameter: 1. 0 mm
Documents :
• Product specification: layout, summary of tissue spots
• H&E stained images
• Detailed pathological information
Layout:
Page 2
Summary of tissue spots
For research use only
(formalin fixed)
A203 ? - Colon cancer tissues
No
Age Sex
Keyword
Differentiation
Dukes
stage
1
1,2
47
m
Adenocarcinoma
wd
C2
2
3,4
64
m
Adenocarcinoma
wd
B2
3
...
[28]
Loss of Tumor Suppressor Gene Triggers Colon Cancer
[149,9 KB]
From [www.hhmi.org] Last viewed: 07.09.2006
Antiproliferative activity of PEP005, a novel agent that activates PKC d and
inhibits PKCa, alone and in combination with cytotoxic agents in human solid
tumor cancer cell lines
Karim A. Benhadji
1
, Maria Serova
2
, Aïda Ghoul
1
, Esteban Cvitkovic
3
, Steven M. Ogbourne
4
,
Peter Welburn
4
, Sandrine Faivre
5
, François Lokiec
1
, Fabien Calvo
2
, Eric Raymond
5
1
Department of clinical Pharmacology, Centre René Huguenin, Saint-Cloud, France;
2
INSERM U716
Saint-Louis Hospital, Paris;
3
CAC Oncology, Le Kremlin Bicetre, France;
4
Peplin Ltd., Newstead,
Australia;
5
Department of Medical Oncology, Hopital Beaujon, Clichy, ...
[29]
Study Links Colon Cancer to Diabetes Drug
[147,2 KB]
From [www.hhmi.org] Last viewed: 07.09.2006
0419
ZNF306, a novel zinc finger transcription factor, drives colon
cancer progression
Lin Yang, Stanley Hamilton, Lee Ellis, Gabriel Lopez-Bernstein,
Angela Sanguino, Douglas Boyd
MD Anderson Cancer Center, Houston, Texas, USA
In colon cancer , simultaneous mutation of the APC , p53 and K- Ras genes
is rare suggesting alternate genetic pathways. UniGene cluster analysis
identified an EST, corresponding to a novel zinc finger protein (ZNF306)
over-represented in colon cancer . RT-PCR confirmed elevated ZNF306
mRNA levels in 7/9 resected tumors. Stable ZNF 306 cDNA expression
in HCT 116 colon cancer cells (wild type p53/APC), increased soft agar
colony formation and 5FU-resistance. In vivo , ZNF306-overexpressing
HCT 116 cells yielded larger tumors than control cells (100 and 20 %
incidence respectively). Transduction of HT29 colon cancer cells with a
ZNF306 ...
[30]
Gene Screen Nabs New Colon-Cancer Genes
[150,2 KB]
From [www.hhmi.org] Last viewed: 07.09.2006
0419
ZNF306, a novel zinc finger transcription factor, drives colon
cancer progression
Lin Yang, Stanley Hamilton, Lee Ellis, Gabriel Lopez-Bernstein,
Angela Sanguino, Douglas Boyd
MD Anderson Cancer Center, Houston, Texas, USA
In colon cancer , simultaneous mutation of the APC , p53 and K- Ras genes
is rare suggesting alternate genetic pathways. UniGene cluster analysis
identified an EST, corresponding to a novel zinc finger protein (ZNF306)
over-represented in colon cancer . RT-PCR confirmed elevated ZNF306
mRNA levels in 7/9 resected tumors. Stable ZNF 306 cDNA expression
in HCT 116 colon cancer cells (wild type p53/APC), increased soft agar
colony formation and 5FU-resistance. In vivo , ZNF306-overexpressing
HCT 116 cells yielded larger tumors than control cells (100 and 20 %
incidence respectively). Transduction of HT29 colon cancer cells with a
ZNF306 ...