[151]
Colon cancer data set (Alon et al., 1999): statistical ...
[25,1 KB]
From [homes.esat.kuleuven.be] Last viewed: 07.09.2006
Colon cancer data set (Alon et al., 1999):
statistical significance tests on test set ROC area
experiments
1
2
3
4
5
6
7
8
9
1
1.000000
0.859650
0.000059
0.513192
0.135862
0.513192
0.211331
0.454919
0.000068
2
0.859650
1.000000
0.000059
0.726978
0.098283
0.726978
0.143702
0.395416
0.000059
3
0.000059
0.000059
1.000000
0.000059
0.000059
0.000059
0.000059
0.000059
0.986130
4
0.513192
0.726978
0.000059
1.000000
0.098547
1.000000
0.156365
0.090576
0.000069
5
0.135862
0.098283
0.000059
0.098547
1.000000
0.098547
1.000000
0.985101
0.000069
6
0.513192
0.726978
0.000059
1.000000
0.098547
1.000000
0.156365
0.090576
0.000069
...
[152]
Colon cancer data set (Alon et al., 1999): statistical ...
[25,9 KB]
From [homes.esat.kuleuven.be] Last viewed: 07.09.2006
Colon cancer data set (Alon et al., 1999):
statistical significance tests on validation set LOO-CV per-
formance
experiments
1
2
3
4
5
6
7
8
9
1
1.000000
0.425781
0.000058
0.001113
0.128135
0.001113
0.192185
0.000167
0.000054
2
0.425781
1.000000
0.000058
0.000854
0.180288
0.000854
0.283767
0.000155
0.000054
3
0.000058
0.000058
1.000000
0.000057
0.000058
0.000057
0.000058
0.000057
0.000036
4
0.001113
0.000854
0.000057
1.000000
0.056524
1.000000
0.044549
0.001953
0.000079
5
0.128135
0.180288
0.000058
0.056524
1.000000
0.056524
1.000000
0.000703
0.000082
6
0.001113
0.000854
0.000057
1.000000
0.056524
1.000000
0.044549
0.001953 ...
[153]
H Colon Cancer:
[99,2 KB]
From [www.comhs.org] Last viewed: 07.09.2006
A
S
P
I
R
E
Foundation, Inc.
Cancer
The Community Hospital
R
ESEARC
H
For the Prevention, Diagnosis and Treatment of Cancer
Volume 2
Issue 2
Summer 2002
Colon Cancer :
Focus on
Detection & Prevention
New initiative seeks to reduce incidence of colon cancer
stronger by the support of local
Cancers of the colon and
The Community Hospital
community groups such as
rectum are the second leading
Cancer Research Foundation,
Ahepa, the Daughters of
cause of cancer deaths in the
with Community Healthcare
Penelope, the John W.
U.S. At least one third of deaths
System, has launched a year-
Anderson Foundation,” said
from colon cancer could be
long
initiative to raise
Donald S. Powers, Chairman
avoided if everyone ...
[154]
Deficient DNA mismatch repair: a common etiologic factor for colon ...
[180,9 KB]
From [courses.washington.edu] Last viewed: 07.09.2006
45
Retinol inhibits the growth of
Retinoic Acid-resistant colon
cancer cells
Presenter
Jessica Leland
Collaborators
Professor Michelle Lane, Alice Dillard, and Erik Wilder, Department of
Human Ecology
Department
Nutrition
Abstract
Retinoids, derivatives of Vitamin A, are responsible for inducing differentiation and
inhibiting cell growth in colon cancer . Retinoic Acid (RA) is unable to inhibit the growth of
cells that become RA-resistant through alteration in metabolism or the loss of retinoic acid or
retinoic “X” receptor activity. We investigated the ability of the more physiologically
relevant retinoid, retinol, to inhibit the growth of RA-resistant colon cancer cell lines,
determined the bioactive metabolites produced within these cells, and the mechanism by
which growth is inhibited. HCT-116, SW620, and WiDr cells were treated with 0 (control),
...
[155]
Effects of TNP-470 on proliferation and apoptosis in human colon ...
[87,9 KB]
From [www.wjgnet.com] Last viewed: 07.09.2006
P.O.Box 2345, Beijing 100023,China
World J Gastroenterol 2003;9(2):281-283
Fax: +86-10-85381893
World Journal of Gastroenterology
E-mail: wjg@wjgnet.com
www.wjgnet.com
Copyright © 2003 by The WJG Press ISSN 1007-9327
•
COLORECTAL CANCER
•
Effects of TNP-470 on proliferation and apoptosis in human colon
cancer xenografts in nude mice
Zong-Hai Huang, Ying-Fang Fan, Hu Xia, Hao-Miao Feng, Fu-Xiang Tang
Zong-Hai Huang, Ying-Fang Fan, Hao-Miao Feng, Fu-Xiang
Tang, Department of Surgery, Zhujiang Hospital, First Military
Medical university, Guangzhou 510282, Guangdong Province, China
Hu Xia, Department of Respiratory Diseases, Zhujiang Hospital, First
Military Medical University, Guangzhou 510282, Guangdong
Province, China
Supported by the Natural Science Foundation of Guangdong
Province, No.013072
Correspondence to: Dr. Zong-Hai Huang, ...
[156]
Teaming Up to Fight Colon Cancer
[846,8 KB]
From [www.miamivalleyhospital.com] Last viewed: 07.09.2006
O N C O L O G Y
S E R V I C E S
Teaming Up to Fight Colon Cancer
Page 2
Dear Colleagues:
Each year in this annual report, we look back at past accomplishments. This year,
we are expanding on that idea and are providing information that physicians, clini-
cians and the general public can use as well. In this report we study colorectal
cancer and share with you Miami Valley Hospital’s approach to fighting this dis-
ease.
I also want to share with you some highlights from 2002:
¦ Miami Valley Hospital was named one of the US News&World Report’s top 50
hospitals in five categories, including gynecology which focuses on fertility
problems and reproductive cancers. Our Gynecologic Oncology Center is the
only program of its kind in the Dayton area. Dr. William Nahhas and his staff are
to be commended.
¦ The Joint Commission ...
[157]
Microsoft PowerPoint - Semi-Automated Imaging in Colon Cancer
[38,6 KB]
From [www.path.ed.ac.uk] Last viewed: 07.09.2006
Semi-Automated Imaging of Human and Mouse Colon Neoplasia
D. Rannie, R. D. G. Malcomson, L.B. Jordon, D. J. Harrison.
Sir Alastair Currie Cancer Research UK Laboratory, Molecular Medicine Centre, Edinburgh EH8 9AG, United Kingdom.
INTRODUCTION
METHODS
IMAGES
ASSESSMENT OF DNA CONTENT
(PLOIDY) BY IMAGE CYTOMETRY.
Aneuploidy within colorectal cancers has
been associated with poor prognosis and
increased likelihood of local recurrence
following resection.
Improved methods for the calculation of
DNA content by image cytometry are bring
new insight
into
the value of ploidy
assessment as an independent prognostic
factor in early stage colorectal cancers.
Automated microscopy and specifically
designed software (Ploidy; Fairfield Imaging)
allow for fast and accurate estimation of DNA
content.
Aim: determine potential as routine clinical ...
[158]
FDA Background for Colon Cancer Endpoints Workshop
[387,4 KB]
From [www.fda.gov] Last viewed: 07.09.2006
FDA Background for Colon Cancer Endpoints Workshop
This document provides FDA background information for a November, 2003 public workshop to
discuss endpoints for the approval of colon cancer drugs.
I.
FDA examination of endpoints for cancer drug approval
The Food and Drug Administration is soliciting input on what endpoints are acceptable as the
basis for cancer drug approval. Endpoints will be examined for the most common cancers, such
as lung cancer , colon cancer , etc. For each cancer , FDA will hold public workshops to identify
important issues, and these issues will be discussed in meetings of the Oncologic Drugs
Advisory Committee (ODAC). Subsequently, guidance documents will be published describing
FDA's current thinking on endpoints for cancer drug approval. Workshop planning is guided by
a steering committee that includes representation from the FDA, the National Cancer Institute, ...
[159]
Direct effects of octreotide, galanin and serotonin on human colon ...
[212,4 KB]
From [147.52.72.117] Last viewed: 07.09.2006
Abstract. The effects of mono, duple and triple treatment
with octreotide, galanin and serotonin on a human colon
cancer cell line (SW 620) were investigated. The cancer cells
were exposed to a dose corresponding to 20 µ g/kg body
weight/day, and to 50 and 25% of this dose (0.2, 0.1 and
0.05 µ g/ml). The cells were observed at the intervals: 3, 6,
12, 24 and 48 h. MTT-assay was used to determine numbers
of viable cells. Proliferation and apoptosis were detected by
immunocytochemistry using the avidin-biotin complex
(ABC) method. The antibodies used were anti-Ki-67, anti-
poly (ADP-ribose) polymerase ‘PARP’ and anti-Bcl-x.
Proliferative and apoptotic indices were determined by
computerized image analysis. Almost all the mono and duple
treatments of the bioactive substances succeeded in reducing
the numbers of viable cells. With triple treatment, however,
this decrease was greater and was evident ...
[160]
EffectsofDNAmethylationonexpressionoftumorsuppressorgenes and ...
[140,4 KB]
From [www.wjgnet.com] Last viewed: 07.09.2006
P.O.Box 2345, Beijing 100023,China
World J Gastroenterol 2003;9(9):1976-1980
Fax: +86-10-85381893
World Journal of Gastroenterology
E-mail: wjg@wjgnet.com
www.wjgnet.com
Copyright © 2003 by The WJG Press ISSN 1007-9327
•
COLORECTAL CANCER
•
EffectsofDNAmethylationonexpressionoftumorsuppressorgenes
and proto-oncogene in human colon cancer cell lines
Jing-Yuan Fang, Juan Lu, Ying-Xuan Chen, Li Yang
Jing-Yuan Fang, Juan Lu, Ying-Xuan Chen, Li Yang, Shanghai
Institute of Digestive Diseases, Renji Hospital, Shanghai Second
Medical University, Shanghai 200001, China
Supported by the National Natural Science Foundation of China,
No.30170413, and Ph.D Funds from the Ministry of Education of
China, No.199946, and the Key Subject Funds of Shanghai Education
Committee to Jing-Yuan Fang
Correspondence to: Dr. Jing-Yuan Fang, Shanghai Institute of ...
[161]
Retinol inhibits the growth of Retinoic Acid-resistant colon ...
[50,7 KB]
From [cns.utexas.edu] Last viewed: 07.09.2006
45
Retinol inhibits the growth of
Retinoic Acid-resistant colon
cancer cells
Presenter
Jessica Leland
Collaborators
Professor Michelle Lane, Alice Dillard, and Erik Wilder, Department of
Human Ecology
Department
Nutrition
Abstract
Retinoids, derivatives of Vitamin A, are responsible for inducing differentiation and
inhibiting cell growth in colon cancer . Retinoic Acid (RA) is unable to inhibit the growth of
cells that become RA-resistant through alteration in metabolism or the loss of retinoic acid or
retinoic “X” receptor activity. We investigated the ability of the more physiologically
relevant retinoid, retinol, to inhibit the growth of RA-resistant colon cancer cell lines,
determined the bioactive metabolites produced within these cells, and the mechanism by
which growth is inhibited. HCT-116, SW620, and WiDr cells were treated with 0 (control),
...
[162]
Aberrant crypt foci and colon cancer: comparison between a short ...
[542,9 KB]
From [www.scielo.br] Last viewed: 07.09.2006
351
Braz J Med Biol Res 35(3) 2002
Aberrant crypt foci and colon cancer
Brazilian Journal of Medical and Biological Research (2002) 35: 351-355
ISSN 0100-879X
Aberrant crypt foci and colon cancer :
comparison between a short- and
medium-term bioassay for colon
carcinogenesis using dimethylhydrazine
in Wistar rats
Departamento de Patologia, Faculdade de Medicina,
Universidade Estadual Paulista, Botucatu, SP, Brasil
M.A.M. Rodrigues,
L.A.G. Silva,
D.M.F. Salvadori,
J.L.V. de Camargo and
M.R. Montenegro
Abstract
Aberrant crypt foci (ACF) in the colon of carcinogen-treated rodents
are considered to be the earliest hallmark of colon carcinogenesis. In
the present study the relationship between a short-term (4 weeks) and
medium-term (30 weeks) assay was assessed in a model of colon
carcinogenesis induced by dimethylhydrazine (DMH) ...
[163]
The angiogenic switch of human colon cancer occurs simultaneous to ...
[190,6 KB]
From [147.52.72.117] Last viewed: 07.09.2006
Abstract. We previously reported that vessel count, vascular
endothelial growth factor (VEGF) and platelet derived endo-
thelial cell growth factor (PD-ECGF) expression are associated
with metastasis formation in human colon cancer . This study
was done to determine a stage of colon cancer progression
where induction of these factors occurred (i.e. the angiogenic
switch). We examined vessel count, VEGF, and matrix
metalloproteinase (MMP)-7 expression in cancer cells and
PD-ECGF expression in infiltrating cells in 25 adenomas,
35 mucosal cancers (Tis), 29 submucosal invasive cancers
(T1) and 33 muscularis propria invasive cancers (T2) by
immunostaining. The intensity of staining of VEGF and
MMP-7 was evaluated blindly at the invasive edge and was
confirmed by image analysis. Intensity of staining for these
factors was graded on a scale of 0 to 3+, with 0 representing
no detectable stain and ...
[164]
Evaluation of telomerase in the development and progression of ...
[85,2 KB]
From [147.52.72.117] Last viewed: 07.09.2006
Abstract. Telomerase activity, a cardinal requirement for
immortalization, is a crucial step in the development of cancer
and has been studied in many kinds of malignant tumours for
clinical diagnostic and/or prognostic utilities. Using a PCR-
based TRAP assay, we investigated telomerase activity in
8 adenomatous polyps, 9 dysplastic polyps, and in 36 paired
cancer -normal mucosa specimens, one liver and one spleen
metastasis from patients resected for sporadic colorectal cancer .
Telomerase was absent or very low in normal mucosa and in
adenomatous polyps. Dysplastic polyps and adenocarcinoma
samples showed telomerase activity, with higher levels in
cancer tissues compared to dysplastic lesions. A high telo-
merase activity was shown to be associated with late-staged
cancers and metastasis, providing arguments supporting the
role of telomerase not only in the development but also in the
progression ...
[165]
Familial Colon Cancer Registry
From [www.huntsmancancer.org] Last viewed: 07.09.2006
What is FAP?
Familial Adenomatous Polyposis
(FAP) is an inherited condition in
which hundreds to thousands of pre-
cancerous or "adenomatous" polyps
form in the colon , usually beginning
at age 16. People with FAP have
almost a 100 percent chance of
developing colon cancer in their
lifetime. However, if a person with
FAP undergoes regular screening
(see guidelines on attached card) and
proper medical management, colon
cancer can almost always be
prevented. FAP occurs when there is
a mutation or change on a gene
called the adenomatous polyposis
Randall W. Burt, M.D.
Director, Colon Cancer Program,
Huntsman Cancer Institute
Registry Coordinators
Familial Adenomatous Polyposis
Spring 2001
What’s Inside:
1-3
Understanding FAP and
AAPC
4
Is genetic testing right for
your family? ...
[166]
Familial Colon Cancer Registry
From [www.huntsmancancer.org] Last viewed: 07.09.2006
at Huntsman Cancer Institute
Familial Colon
Cancer Registry
Everyone is touched by
inheritance in some way; you may
have been told that you have your
father’s smile, your mother’s sense of
humor, or your uncle’s nose. It is
easy to think of examples when it
comes to physical or personality
traits. At the Registry, we are in the
business of thinking about the
inherited nature not of personality
or appearance, but of polyps, colon
cancer and related cancers. We want
to learn more about the causes,
prevention, and treatment of cancer
by studying syndromes or trends in
families like yours. We have invited
several groups into the Registry -
each will help us focus on different
aspects of cancer . The goal of this
article is to help you understand the
scope of the Registry and how you
fit into our resource.
What are genes? ...
[167]
Familial Colon Cancer Registry
From [www.huntsmancancer.com] Last viewed: 07.09.2006
at Huntsman Cancer Institute
Familial Colon
Cancer Registry
We thank all of you who are considering participation in our Colon Registry. The purpose of the
Registry is three-fold: 1) to keep you up to date on the research and advances important to your
care; 2) to let you know of research projects that you may be interested in joining; and, 3) to assist
in clinical care associated with risk for inherited or familial polyps, colon cancer and related
cancers.
It is an exciting time in the area of genetics pertaining to cancer . The involved genes are known
for many of the inherited cancer syndromes making genetic testing available to determine who
does and does not have one of the syndromes. In addition, most cancers in this category can now be
prevented through proper screening.
We also continue to look at new prevention strategies and therapies. For example, medications
that cause ...
[168]
Voltage-gated potassium ion channels in colon cancer
[177,3 KB]
From [147.52.72.117] Last viewed: 07.09.2006
Abstract. Voltage-gated potassium channels (VGPCs) have
been previously implicated in cellular proliferation. In this
study, the expression of VGPCs was examined by immuno-
histochemistry in seventy-four human colonic carcinoma
specimens. Immunostaining for the Kv1.3 type VGPC was
absent in two normal human colon specimens. Kv1.3 staining
in the 74 colon cancer specimens was low in 9% (7/74),
moderate in 61% (45/74) and high in 30% (22/74). Potassium
channel (PC) openers, minoxidil and diazoxide (5-50 µ g/ml),
increased growth of SW1116, LoVo, Colo320DM and LS174t
human colon cancer cell lines by 20-40%. PC-blockers,
dequalinium and amiodarone, caused marked growth-
inhibition of the four cell lines, at concentrations between
1 to 3 µ g/ml. PC-blockers such as glibenclamide inhibited
cellular proliferation at concentrations above 50 µ g/ml while
tetraethylammonium and 4-aminopyridine (up ...
[169]
Neoangiogenesis in colon cancer: Correlation between vascular ...
[22,7 KB]
From [147.52.72.117] Last viewed: 07.09.2006
Abstract. Angiogenesis is an essential requirement for the
development, progression and metastasis of malignant
tumors. Vascular endothelial growth factor (VEGF) plays an
essential role in the development of angiogenesis of numerous
solid malignancies, including colon cancer . The tumor
suppressor gene p53 is a potent transcriptional regulator of
genes which are involved in many cellular activities, including
cell-cycle arrest, apoptosis and angiogenesis. In order to
better understand the relation among p53 status, VEGF
expression and microvessels count (MVC) in colon cancer ,
we evaluated immunoreactivity for CD34 endothelium-
associated antigen, VEGF and p53 proteins in 43 cases of
colon adenocarcinoma. Our results demonstrated an association
between VEGF expression, p53 status and angiogenesis,
suggesting that mutant p53 plays a central role in promoting
angiogenesis in colon cancer ...
[170]
(pdf) Colon Cancer Screening Program
[35,2 KB]
From [www.queens.org] Last viewed: 07.09.2006
Cancer Services
Colon Cancer Screening Program
Colon cancer is the number two cause of death from cancer in the United
States. About 131,000 men and women will get cancers of the colon this
year. Most people get it after age 50. But if you take 10 minutes of your
time to screen today, you may save your life tomorrow.
Why is it Important to Find Colon Cancer Early?
Colon cancer is much easier to cure when found early. By doing so, we can
prevent 80% of colon cancer deaths. Finding cancer early could:
• Save your life
• Avoid later surgeries
What if I Feel Just Fine?
If you are 50 or older, this is the best time to get a colon cancer screening
test. In its early stage, colon cancer does not cause any symptoms or pain.
Screening tests help find problems early -- long before you would notice
something wrong.
What is Done ...
[171]
Case #4 Sentinel Node Biopsy in Colon Cancer
[183,3 KB]
From [www.facs.org] Last viewed: 07.09.2006
Case #4 Sentinel
Node Biopsy in
Colon Cancer
David M. Ota, MD, FACS
Milwaukee, WI
Page 2
65 yo female with sigmoid
adenoca. CXR, liver US and
CEA are normal. Sigmoid
colectomy done and final path
report shows T3 with 6 negative
lymph nodes(T3N0M0).
Page 3
Pathologic
Understaging
of CRC
reality or fiction?
Page 4
Colon Cancer
5 yr survival
stage I 90-95%
stage II 80%
stage III 50-60%
Page 5
Stage II Colon Ca
1016 pts in 5 adjuvant
trials
5 yr survival
obs 80%
FU+LV 82%
Impact Invest JCO 1999
Page 6
Stage III improved
survival with FU+LV
Some Stage II are
understaged
Page 7
Standard Technique
1. ...
[172]
Identifying gene variants may help evaluate colon cancer risk ...
[182,4 KB]
From [www.usc.edu] Last viewed: 07.09.2006
Vol. 8, No. 12
April 19, 2002
Identifying gene variants may
help evaluate colon cancer risk
Keck School of Medicine oncologists recently
took their research on the road, sharing results
from their studies on genetic variations and their
relationship to colon cancer patients’ outcomes.
Heinz-Josef Lenz, associate professor of med-
icine, and researchers in his lab at the
USC/Norris Comprehensive Cancer Center
reported that certain polymorphisms in genes
might help direct treatment choices or potential-
ly provide a way to tip off people at high risk of
developing cancer .
The researchers reported their findings at the
93rd annual meeting of the American
Association for Cancer Research, held from April
6 to 10 in San Francisco.
The investigators are looking into three
genes: thymidylate synthase, or TS; glutathione
S-transferase P1, or GSTP1; and ...
[173]
New Technologies to Improve Cancer Diagnosis and Treatment Colon ...
[27,7 KB]
From [www.advamed.org] Last viewed: 07.09.2006
New Technologies to Improve Cancer Diagnosis and Treatment
Breakthroughs in cancer diagnosis and treatment are helping save more patients’ lives
than ever before. National Cancer Institute statistics show the cancer death rate is falling
by more than 1% each year. Advances in technology are not only saving peoples’ lives
but also helping improve the productivity of our health care system and reduce overall
costs. Many of these exciting innovations are on display at the National Dialogue on
Cancer event Cancer Research: New Technology’s Role in Diagnosis and Treatment.
Colon Cancer
Colorectal cancer often is diagnosed late and results in death. It is estimated that there
will be 138,900 new cases in 2001 with a projected death toll of 57,100. Even though
colorectal cancer is most curable if detected in the early stages, many Americans are
failing to be screened for colorectal ...
[174]
Familial Colon Cancer Registry
From [www.huntsmancancer.org] Last viewed: 07.09.2006
distinguishes this syndrome from
another inherited condition, called
Familial Adenomatous Polyposis
(FAP), in which individuals develop
hundreds or thousands of polyps,
while people with HNPCC may only
develop a small number of polyps.
Individuals who have HNPCC have
an 80 percent lifetime risk of
developing colon cancer . However, it
is important to note that not all
individuals with HNPCC will
develop colon cancer . In HNPCC,
colon cancer occurs around age 44,
whereas the statistical average for a
diagnosis of colon cancer is about age
65. With regular screening (see
“Screening Recommendations” on
page 3) and appropriate medical
management, colon cancer can
almost always be prevented.
What are colon polyps?
Polyps are abnormal growths that
form on the inside lining of the
by Lisa Bredthauer
High Risk Registry Coordinator ...
[175]
5 Cancer of the colon
[456,2 KB]
From [www.aihw.gov.au] Last viewed: 07.09.2006
24
5 Cancer of the colon
Summary
In 1992–1997 relative survival one year after diagnosis was 77.6% for males and 76.0% for
females. Five-year relative survival proportions were 58.3% and 58.7% for males and
females, respectively (Table 5.1). Survival ten years after diagnosis was 51.0% for males and
52.0% for females in 1987–1991, the most recent period for which ten-year relative survival
data are available (Tables 5.2 and 5.3).
Relative survival after diagnosis of colon cancer increased significantly between 1982–1986
and 1992–1997 diagnostic periods. Increases in relative survival have been statistically
significant for all relative survival times (including one-, five- and ten- year relative survival)
for males and females. Five-year relative survival increased by 8.1 percentage points for
males and 7.4 percentage points for females between 1982–1986 and 1992–1997 (Figure 5.2;
Tables ...
[176]
Genetic testing for colon cancer: Joint statement of the American ...
[65,4 KB]
From [www.acmg.net] Last viewed: 07.09.2006
Genetic testing for colon cancer : Joint statement of
the American College of Medical Genetics and
American Society of Human Genetics
Joint Test and Technology Transfer Committee Working Group
Colorectal cancer (CRC) is the second leading cause of can-
cer death in the United States. Annually, approximately
130,200 individuals will be diagnosed and 56,300 will die from
this disease.
1
In general, CRC evolves in an “adenoma to car-
cinoma” sequence during which a series of somatic alterations
accumulate in the DNA of the tumor tissue. Since 1987, signif-
icant strides have been made in characterizing the genetic
events that lead to colorectal cancer . This work has been based
on detailed clinical and molecular genetic studies of colorectal
tumors. Acquired genetic alterations seen in tumors include
APC and MCC on chromosome 5q, KRAS on chromosome
12p, DCC on chromosome ...
[177]
Could Wheat Bran Fight Colon Cancer? It’s long been known that raw ...
[9,5 KB]
From [www.ars.usda.gov] Last viewed: 07.09.2006
Agricultural Research/November 1997
23
Could Wheat Bran Fight Colon
Cancer ?
It’s long been known that raw
wheat bran helps laboratory animals
battle colon cancer . Now, ARS
scientists and colleagues from
Kellogg Co., Battle Creek, Michigan,
have teamed up to find out if pro-
cessed wheat bran can have a similar
effect.
Bran is the thin outer layer of the
wheat kernel. Processed bran is found
in breakfast cereals, whole-wheat
breads, and other foods. The new
research is being conducted under a
cooperative research and develop-
ment agreement.
Earlier medical studies found that
lab animals fed raw wheat bran have
fewer aberrant colonic crypt cells.
These cells are thought to be pre-
cancerous, and no one knows exactly
how raw bran reduces their
formation.
The ARS scientists are experi-
menting with samples of bran pro-
cessed ...
[178]
6. MALIGNANT CANCER OF THE COLON
[145,6 KB]
From [www.allirelandnci.org] Last viewed: 07.09.2006
All-Ireland cancer statistics 1994-96
43
Colon
6. MALIGNANT CANCER OF THE COLON
ICD-O.2 C18
ICD-10 C18
ICD-9 153
This site includes the colon , from caecum and appendix to sigmoid colon , but excludes the rectosigmoid junction and overlapping
tumours of colon and rectum. See also Chapters 5 (colorectal cancer , including all sites from colon to anus) and 7 (anorectal cancer ).
Key facts
•
Average of 1702 new cases per year, 1994-96: 826 in females, 876 in males.
•
Average of 1025 deaths per year: 490 in females, 535 in males.
•
Age-standardised rates higher in males than females, by about 38% (incidence), about 51% (mortality).
•
3rd most common site for cancer incidence in females, 4th most common in males.
•
3rd most common cause of cancer deaths in both sexes.
•
Higher incidence rates in Northern Ireland (NI) ...
[179]
Colon Cancer
[540,3 KB]
From [rcctvm.org] Last viewed: 07.09.2006
Colon Cancer
(Page 1 of 3)
ADJUVANT
THERAPY
PRIMARY
TREATMENT
PATHOLOGIC FINDINGS
INITIAL
EVALUATION*
CLINICAL
PRESENTATION
PATHOLOGIC
STAGE
Completely
removed
CIS
Adenomatous polyp
with noninvasive
carcinoma (CIS)
Adenomatous polyp
with invasive cancer
Ulcerative/invasive
nonobstructing
lesion
Residual
adenoma
Repeat colonoscopy
immediately
Surveillance
Resectable
Unresectable
Stage I
T1-2
N0 M0
Stage II
T3-4 N0 M0
Poorly differentiated or fragmented
specimen or T2 or greater or lymph
or vascular invasion or residual lesion
or mass
T1, margins negative well or
moderately differentiated, no
lymph or vascular invasion,
and no residual lesion or mass
Stage III
T1-3 N1-2
M0
Stage III
T4 ...
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Expression of Estrogen Receptor (ER) Subtypes and ER Isoforms in ...
[567,8 KB]
From [www.pathology.ufl.edu] Last viewed: 07.09.2006
[ CANCER RESEARCH 61, 632–640, January 15, 2001]
Expression of Estrogen Receptor (ER) Subtypes and ER Isoforms in
Colon Cancer
1
Martha Campbell-Thompson,
2
I. Jeanette Lynch, and Bhavna Bhardwaj
Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida 32610
ABSTRACT
Colon cancer incidence and mortality rates are lower in females com-
pared with males, and numerous epidemiological studies suggest that
estrogen replacement therapy (ERT) reduces cancer risk in postmeno-
pausal women. Two estrogen receptor (ER) subtypes, ER and ER ,
mediate genomic effects in target cells. The aim of this study was to
determine the relative mRNA expression levels for ER subtypes and ER
isoforms in colon tumors, normal colonic mucosa, and colon cancer cell
lines. ER and ER isoform mRNA levels were investigated ...