Académique Documents
Professionnel Documents
Culture Documents
S amygdala
Tumor-host cell interactions in the bone disease
Many researchers will only read the abstract so
Must give an accurate summary of your research,
and enough information so that readers can
understand:
What you did
Why you did it
What your findings are
Why your findings are useful and important
Edanz Group Ltd. | 20
Abstract
General rules for abstracts:
Within the word limit
Avoid technical jargon
Avoid abbreviations unless necessary
Avoid references
Structured or unstructured?
A C A
determine allowable length, style and abbreviations
Edanz Group Ltd. | 21
Abstract
Edanz Group Ltd. | 22
Abstract Structured
Risk factors and mortality in patients with nosocomial staphylococcus aureus bacteremia
BACKGROUND: Infections due to methicillin-resistant Staphylococcus aureus have become
increasingly common in hospitals worldwide. S aureus continues to be a cause of
nosocomial bacteremia.
METHODS: We analyzed the clinical significance (mortality) of MRSA and methicillin-
susceptible S aureus bacteremia in a retrospective cohort study in a 2900-bed tertiary
referral medical center. Survival and logistic regression analyses were used to determine
the risk factors and prognostic factors of mortality.
RESULTS: During the 15-year period, 1148 patients were diagnosed with nosocomial S
aureus bacteremia. After controlling potential risk factors for MRSA bacteremia on logistic
regression analysis, service, admission days prior to bacteremia, age, mechanical ventilator,
and central venous catheter (CVC) were independent risk factors for MRSA. The crude
mortality rate of S aureus bacteremia was 44.1%. The difference between the mortality
rates of MRSA (49.8%) and MSSA bacteremia (27.6%) was 22.2% (P < .001). Upon logistic
regression analysis, the mortality with MRSA bacteremia was revealed to be 1.78 times
higher than MSSA (P < .001). The other predicted prognostic factors included age,
neoplasms, duration of hospital stay after bacteremia, presence of mechanical ventilator,
and use of CVC.
CONCLUSIONS: Resistance to methicillin was an important independent prognostic factor
for patients with S aureus bacteremia.
PMID: 18313513 [PubMed - indexed for MEDLINE]; Am J Infect Control. 2008
Mar;36(2):118-22.
2 sentences
2 sentences
5 sentences
1 sentence
Abstracts are often followed by a list of keywords
selected by the authors
Choosing appropriate keywords is important for
indexing purposes
Your manuscript can more easily identified,
read and cited
Keywords should be specific to your manuscript
General terms should be avoided
Many medical journal require MeSH terms
Edanz Group Ltd. | 23
Keywords
Manuscript title:
Region-specific neuronal degeneration after okadaic acid
administration
Poor keywords:
neuron, brain, OA (as an abbreviation), regional-specific
neuronal degeneration, signaling
Better keywords:
okadaic acid, hippocampus, neuronal degeneration,
MAP kinase signaling
Edanz Group Ltd. | 24
Keywords
Must give the reader enough background information
to put your work into context
Enough information to understand the rationale for
your study is all that is required
Do not write a comprehensive literature review of the
field
Do cite reviews that readers can refer to if they want
more information
Edanz Group Ltd. | 25
Introduction
Define technical and non-familiar terms
hypotheses to explain the rationale for the study
Briefly explain how you addressed this problem
and what was achieved (12 sentences for each)
Citations must be balanced, current and relevant
Edanz Group Ltd. | 26
Introduction
Introduction
Liver resection has become an increasingly safe procedure, but certain
procedures remain high risk, such as massive liver resection and small-for-
size (SFS) liver transplantation. Massive hepatic resection is the only option
The failure of a partial liver to regenerate is considered a critical contributing
factor in postsurgical primary liver dysfunction and liver failure, and minimal
viable liver volume required for regeneration, following either massive liver
resection or SFS transplantation, is an important concept...
Thus, although the studies outlined above indicate that complement
inhibition represents a potential therapeutic strategy to protect against
hepatic IRI, the important role of complement in liver regeneration would
appear to be a contraindication for such a strategy in the context of liver
resection and SFS liver transplantation, even though IRI is associated with
In the current study, we investigated the role of complement in the
relationship between hepatic IRI and liver regeneration using 3 murine
models: a warm total hepatic IRI model (similar to the Pringle maneuver), a
70% PHx model, and a combined IRI/PHx model designed to recreate clinical
massive liver resection under the Pringle maneuver. In these studies, we
used the complement inhibitor CR2
Edanz Group Ltd. | 27
A complement-dependent balance between hepatic
ischemia/reperfusion injury and liver regeneration in mice
Songqing He, Carl Atkinson, Fei Qiao, Katherine Cianflone, Xiaoping Chen and Stephen Tomlinson
The Journal of Clinical Investigation (doi:10.1172/JCT38289; reproduced with permission)
Statement of the problem
Background
Rationale
What was done
Clear subheadings for methods/materials
Describe methods in the past tense
Novel methods must be described in sufficient detail
for a capable researcher to reproduce the experiment
Give manufacturers/suppliers and their locations
Describe any statistical tests used
Established methods can be referenced
Edanz Group Ltd. | 28
Materials and methods What you did
Edanz Group Ltd. | 29
Proapoptotic signaling induced by RIG-I and MDA-5 results in type I
interferon-independent apoptosis in human melanoma cells.
Robert Besch, Hendrik Poeck, Tobias Hohenauer et al.
Reagents and antibodies. Anticaspase-3, anticaspase-8 (1C12), anticaspase-9, antiBcl-x
L
, antiBcl-w,
and HRP-conjugated secondary antibodies were obtained from New England Biolabs. Anticytochrome c
(clone 7H8.2C12) was from BD Biosciences. Anti-Noxa (N-15) antibody was from Santa Cruz Biotechnology
Inc. AntiBcl-2 (Ab-1) and anti-p53 (Ab-6) antibodies were from Merck Biosciences. AntiIPS-1 antibody
was obtained from Bethyl Laboratories Inc. Anti-actin (AC-15) and anti-Puma (bbc3) antibodies were
purchased from Sigma-Aldrich. PCR primers and siRNAs were purchased from MWG Biotech.
Immunostimulatory and siRNAs. Poly(I:C) was purchased from Amersham Biosciences. 5-Triphosphate
conjugated RNAs (pppRNAs) were transcribed in vitro from DNA templates as described in ref. 6. They
contained a T7 RNA Polymerase consensus promoter sequence followed by the sequence of interest to be
transcribed (MEGAshortscript Kit; Ambion). Reactions were treated with DNAse I (Ambion
siRNAs were designed according to published guidelines (48, 49) 3 Overhangs were carried out as two
deoxythymidine residues (dTdT). Sequences of specific siRNAs are listed in Supplemental Table 1.
Nonsilencing control siRNAs were designed to contain random sequences that do not match within the
human genome...
Cell culture. Human melanoma cell lines were a gift of M. Herlyn (Wistar Institute, Philadelphia,
uSA
Analysis of lung metastasis. For metastasis analysis at day 10, we isolated genomic DNA from lungs.
Mouse lungs were reduced to small pieces and digested overnight at 56C in a buffer containing 10 mM
Tris, pH 8.0, 100 mMNaCl, 1 mMEDTA, 1% SDS, 0.5 mg/ml Pronase E (Sigma-Aldrich), and 150 /ml
Protease K (Sigma-Aldrich). Genomic DNA was purified by phenol/chloroform extraction. The amount of
human and murine DNA was determined by quantitative PCR using the LightCycler TaqMan Master Kit
(Roche) together with the Universal Probe Library system (Roche). A 72-bp portion in the second intron of
-actin
Statistics. For statistical analysis, 2- S t test was used to assess the significance of mean
differences. Differences were considered significant at a P value of 0.05 or less.
Materials
described
first
References
to save
space
Clear
subheadings
Detailed
information
given
Suppliers
Statistical
test
information
The Journal of Clinical Investigation (doi:10.1172/JCI37155; reproduced with permission)
A
Present your findings in subsections (the same as those in your
methods section)
Present complementary evidence when possible
Describe results in the past tense
Refer to figures and tables in the present tense
Do not discuss implications do that in the discussion section
Do not duplicate data among figures, tables and text
Show the results of statistical analyses, (e.g., p values) in the
text
Edanz Group Ltd. | 30
Results What did you find?
Edanz Group Ltd. | 31
Proapoptotic signaling induced by RIG-I and MDA-5 results in type I
interferonindependent apoptosis in human melanoma cells
Robert Besch, Hendrik Poeck et al
pppRNA and poly(I:C) induce apoptosis in melanoma cells.
We tested the ability of RIG-I and MDA-5 ligands to induce cell death in human melanoma cell lines. Five cell
lines derived from advanced melanomas (vertical growth phase or metastatic origin) were analyzed.
Activation of RIG-I and MDA-5 by pppRNA1 and poly(I:C) strongly reduced viability from 100% in controls to
20%50% within 24 hours l lA1 A). Viability was reduced due to induction of apoptosis as
determined by staining with annexin V. Apoptosis strictly required intracellular delivery, as neither pppRNAs
nor poly(I:C) without transfection were active l l81 B). Different pppRNAs were tested, and all
reduced cell viability l lC1 C) 1 -triphosphate moiety was required, since synthetic RNAs
CP CP-RNA1) had no effect l lC1 C, left panel). Strong
dose-dependent reduction of viability was observed for poly(I:C) l lC1 C, right panel). Reduced
viability was reflected in an increased number of cells undergoing apoptosis l lu1 D).
Confirming the onset of apoptosis, caspase-3 was activated in cells transfected with pppRNAs or poly(I:C) but
not in cells exposed to pppRNA or poly(I:C) in the absence of transfection reagent l lL1 E).
Together, these results show high sensitivity of human melanoma cell lines toward apoptosis induction by
pppRNAs or poly(I:C) when delivered to the cytosol.
Apoptosis induction by pppRNA and poly(I:C) involves IPS-1 but is independent of IFN signaling.
The RNA ligands pppRNA and poly(I:C) both induced IFN-
l lAA S 8lC-I and MDA-5 confirmed that induction of IFN- pppRNA and
poly(I:C) required RIG-I and MDA-5, respectively, and that both
Melanoma cells are more sensitive to RIG-I and MDA-5induced apoptosis than primary cells.
We next compared healthy primary cells of the skin with melanoma cells to evaluate tumor specificity of
apoptosis induction by RIG-I and MDA-5. Primary human melanocytes, primary fibroblasts, and primary
keratinocytes were significantly less sensitive to pppRNA and poly(I:C) compared with melanoma cells
l lAA
Graphics used to
show data with
only brief
descriptions in
text
Clear
subheadings
It is clear what
was compared
with what
The Journal of Clinical Investigation (doi:10.1172/JCI37155; reproduced with permission)
Some readers will only look at the figures and their legends
Figures and tables are the best way to present your results
Data shown in figures and tables must be easy to interpret use separate
panels if necessary
Avoid redundancies or duplication
Clearly label all components
Show trendlines, scale bars and statistical significance
L
(except when describing methods)
Comply with journal guidelines on display items
Edanz Group Ltd. | 32
Display items Tables and figures
Tables are a great way to present large amounts of necessary
data with minimal description required
Part of a table in a paper published in The Journal of Clinical Investigation (doi:10.1172/JCI37622; reproduced with permission)
Edanz Group Ltd. | 33
Display items Tables and figures
Clear concise heading
Data divided into
categories for
clarity
Percentages as well as
absolute values
Edanz Group Ltd. | 34
Display items Tables and figures
Trend lines
Multi-panel:
different kinds of
data grouped
together in a single
figure
Complicated data
separated into
simpler components
Scale bars
Figure 5
RCP knockdown attenuates
tumor formation and metastasis.
Effects of RCP inhibition on
tumor growth using (A) MCF7
cells in nude mice and (B) MB231
cells in NOD-SCID mice are
shown. (A) Left panel shows
mean tumor volume plotted as a
function of time (mean SEM).
Right panel shows tumor weight
plotted at 5 weeks; mean weight
indicated by solid line. (B) Left
panel, tumor weight plotted at
indicated number of weeks;
mean weight indicated by solid
line. Right panel, the average
number of lung micrometastases
per section is shown. (C)
Representative lung sections and
fluorescently imaged whole lungs
(right panel) of NOD-SCID mice
are shown. Micrometastases are
indicated by arrows. Scale bars:
200 .
C
The Journal of Clinical Investigation (doi:10.1172/JCI37622; reproduced with permission)
Edanz Group Ltd. | 35
Statistics
A
1
He is comfortable
Today, few professional activities are untouched by
statistical thinking, and most academic disciplines use it
S
observations of the world can never be totally accurate;
Rowntree D (1981). Statistics without tears. A primer for non-mathematicians. Penguin Books Ltd., London,
England
Edanz Group Ltd. | 36
Statistics
Statistical analysis is at the heart of scientific inquiry
Consider statistical analysis when you design your
study. Before you start your research.
Edanz Group Ltd. | 37
Statistics
Data
collection
Data
analysis
Interpretation
Edanz Group Ltd. | 38
Statistics Poor statistics
Poor statistics
Poor study
design
e.g., sample
size is too small
Poor analysis
Data are valid
Re-analysis or re-interpretation
Revise manuscript
Poor interpretation
Reporting statistics in your manuscript:
Consult a statistical expert about which test to use!
Clearly describe the statistical tests used to analyze
data
Give the software, version number and maker
Only
statistically significant differences
Alternatives: notable, substantial, marked
u
Edanz Group Ltd. | 39
Statistics Basics
Edanz Group Ltd. | 40
Statistics Questions
Ask yourself these questions during study design:
What are the independent and dependent variables?
What is the scale of measurement of the study
variables?
Consider sample number for power analysis
i.e., how many samples will you need?
Have I met the assumptions of the statistical test
selected?
Edanz Group Ltd. | 41
Statistics Details
Reporting statistics in your manuscript:
l meansS.D
Give the numerator and denominator with
8
Book
As a full guide see the excellent book:
How to report statistics in medicine
by Thomas A. Lang and Michelle Secic (ACP Press, Second Edition)
C
8Ml
Figure 7
Opposing effects of high- and low-dose complement inhibition on hepatic injury and regeneration in a model incorporating both IRI
and PHx. Mice were treated with normal saline or CR2-Crry at a dose of either 0.25 mg or 0.08 mg immediately after surgery. C3
/
mice received no treatment. All determinations made 48 hours after I/R and PHx. (A) Mouse survival. (B) Serum ALT levels. (C)
Histological quantification of hepatic necrosis and injury determined on a scale of 04. (D) Assessment of regeneration by BrdU
incorporation. (E) Restitution of liver weight. (F) MPO content in liver samples.
#
P < 0.05,
##
P < 0.01 versus WT group; **P < 0.01
versus WT group (similar to WT normal saline group);
P < 0.01 versus all other groups; *P < 0.05, **P < 0.01 versus WT group.
Results are expressed as mean SD; n = 610.
A complement-dependent balance between hepatic ischemia/reperfusion injury
and liver regeneration in mice
Songqing He, Carl Atkinson et al
Edanz Group Ltd. | 43
The Journal of Clinical Investigation (doi:10.1172/JCI38289; reproduced with permission)
Statistics. Data are expressed as mean SD. Significant
differences between groups were determined by ANOVA, with
a Bonferroni correction for continuous variable and multiple
groups. Two- S t test was used for the
comparison of a normally distributed continuous variable
between 2 groups. For the survival studies, Kaplan-Meier log-
rank analysis was performed. P values of less than 0.05 were
considered statistically significant.
ALT levels were significantly lower at 24 and 48 hours after PHx in
low-dose CR2-Crrytreated mice compared with those in saline-
Compared with WT mice, surviving C3
/
mice had significantly
increased hepatic injury and an impaired proliferative response
(Figure 7, BE)...
Methods Results
Data type defined Statistical tests clearly described
statistical significance
Significance indicated in figure/table legend
Significance threshold defined
Restate your research question and/or any hypotheses
presented in the introduction
Summarize your main findingsmake it clear how your
study has advanced the field
Begin with your most important finding
Past tense to describe results (current and published)
Present tense to describe their implications
Minimize repetition with other sections
Describe inconsistencies with other papers
Describe the limitations of your study
Edanz Group Ltd. | 44
Discussion What does it all mean?
Be humble
u overstate the importance of your results
Our findings prove that
Our findings show
Our findings suggest
Edanz Group Ltd. | 45
Discussion
Restate key findings and their significance
Propose future studies that might follow on from your
current study
C -home
Edanz Group Ltd. | 46
Conclusions
Science)
P
concerns and reinforce the efficacy of tropical antimicrobial therapy Curr
Infect Dis Rep)
-
protein and protein-unA (Nature)
Discussion
Genome-wide microarray analysis of primary tumors has enabled the discovery of novel, clinically
relevant tumor subtypes defined by unique patterns of gene expression. More recently, however,
the inverse of this concept has been explored through bottom-up analytical strategies that seek to
identify gene subtypes with functional roles in tumorigenesis
In the present work, we have built on this concept of data integration and functional discovery and
identified RCP, located on the 8p1112 recurrent breast cancer amplicon, as a novel breast-cancer
promoting gene with Ras-
Amplification of the 8p1112 locus has been observed in approximately 10%25% of breast tumor
cases and 15% of breast cancer cell lines and has been associated with poor patient survival and
short interval to distant metastasis. Recently, this amplicon has been the focus of several
functional genomics investigations involving primary breast tumors and cell lines. Using a high-
resolution BAC microarray specific for chromosome 8p, Gelsi-8
However, that the growth and metastatic properties of the tumor xenografts were dependent on
the endogenous expression of RCP suggests oncogene addiction 8C
may play a vital role in the maintenance and potentiation of the malignant and metastatic