---
title: "Pancreatic Cancer"
output: html_vignette
vignette: >
  %\VignetteIndexEntry{Data: Pancreatic Cancer}
  %\VignetteEngine{knitr::rmarkdown}
  \usepackage[utf8]{inputenc}
bibliography: data_sources.bib
csl: peerj.csl
---

This [<span style="color:red;text-decoration:underline">vignette</span>](http://chnosz.net/canprot/doc/index.html) from the R package [canprot](http://github.com/jedick/canprot) reproduces calculations of compositional oxidation state and hydration state that are described in a paper published in _PeerJ_ ([Dick, 2017](https://doi.org/10.7717/peerj.3421)).

## Abbreviations
T (tumor), N (normal), CP (chronic pancreatitis), AIP (autoimmune pancreatitis), PC (pancreatic cancer), DM (diabetes mellitus), PDAC (pancreatic ductal adenocarcinoma), ANT (adjacent normal tissue), FFPE (Formalin-fixed paraffin-embedded), LCM (laser-capture microdissection), NP (normal pancreas).

## Summary Table

This table compares the chemical compositions of groups of human proteins that are relatively down- and up-expressed (`n1` and `n2`, respectively) in pancreatic cancer compared to non-tumor tissue.

```{r options, echo=FALSE}
options(width = 90)
```

```{r canprot, message=FALSE}
library(canprot)
```

```{r datasets}
datasets <- pdat_pancreatic()
```

```{r comptab, message=FALSE}
comptab <- lapply_canprot(datasets, function(dataset) {
  pdat <- get_pdat(dataset, "pdat_pancreatic")
  get_comptab(pdat, plot.it=FALSE, mfun="mean")
}, varlist="pdat_pancreatic")
```

```{r xsummary, results="asis"}
library(xtable)
xsummary(comptab)
```

## Data Sources

<b>a</b>. Pooled tissue samples of PC and matched normal tissue from 12 patients. Source: Tables 2 and 3 of @LHE+04.
<b>b</b>. Two PC and two normal pancreas samples. Source: Tables 1 and 2 of @CYD+05.
<b>c</b>. Large-scale immunoblotting (PowerBlot) of 8 tissue specimens of pancreatic intraepithelial neoplasia compared to normal pancreas and CP. Source: Table 2 of @CGB+05.
<b>d</b>. Tissue specimens from patients with CP (without any findings of pancreatic cancer) and 10 control specimens from patients with normal pancreas. Source: Table 1 of @CBP+07.
<b>e</b>. 12 carcinoma samples (PDAC), 12 benign pancreatic adenocarcinomas and 10 normal tissues adjacent to the PDAC primary mass. Source: Table 1 of @CTZ+09.
<b>f</b>. Source: extracted from Suppl. Table S2 of @MLC+11.
<b>g</b>. PDAC compared to normal pancreas. Source: Suppl. Table 3 of @PCS+11.
<b>h</b>. Potentially accessible proteins in fresh samples of PC tumors (three patients) vs normal tissue (two patients with normal pancreas and one with CP). Source: extracted from the SI Table of @TMW+11.
<b>i</b>. 11 tissue specimens containing >50% cancer and 8 unmatched, uninvolved tissues adjacent to pancreatitis. Source: Suppl. Tables 2 and 3 of @KBK+12.
<b>j</b>. Fresh-frozen PDAC tissue specimens from 7 patients vs a pooled mixture of 3 normal main pancreatic duct tissue samples. Source: extracted from SI Table S3 of @KHO+13, including proteins with an expression ratio >2 [or <0.5] in at least 5 of the 7 experiments and ratio >1 [or <1] in all experiments.
<b>k</b>. Frozen samples of PDAC tumors vs adjacent benign tissue from four patients. Source: Suppl. Table 2 of @KPC+13.
<b>l</b>. <b>m</b>. Tissue samples from 3 patients with PC vs 3 patients with AIP or 3 patients with CP. Source: extracted from Tables 2, 3, and 4 of @PKB+13.
<b>n</b>. <b>o</b>. 12 samples each (pooled) of low-grade tumor or high-grade tumor vs non-tumor. Source: extracted from Suppl. Tables S4 and S5 of @WLL+13, including proteins with ratios ≥1.5 or ≤0.667 for at least 2 of the 4 groups, and with expression differences for all 4 groups in the same direction.
<b>p</b>. <b>q</b>. Source: extracted from Suppl. Tables S3 and S4 of @WLL+13a, including proteins with >3/2 or <2/3 fold change in at least 3 of 4 iTRAQ experiments for different pooled samples.
<b>r</b>. LCM of CD24<sup>+</sup> cells from PDAC vs CD24<sup>-</sup> cells from adjacent normal tissue (ANT). Source: SI Table S5 of @ZNWL13.
<b>s</b>. Matched PDAC and normal tissue from nine patients. Source: extracted from SI Table S5 of @ISI+14, excluding proteins marked as "not passed", i.e. having inconsistent regulation.
<b>t</b>. PDAC tumors in transgenic mice vs pancreas in normal mice, analyzed at time points of 2.5, 3.5, 5 and 10 weeks. Source: Suppl. Table of @KKC+16.

## Mean Differences

The datasets comparing chronic pancreatitis or low-grade tumor to normal proteomes are highlighted in red.

```{r diffplot, fig.width=6, fig.height=6, fig.align="center"}
col <- rep("black", length(datasets))
col[grepl("=low", datasets)] <- "red"
diffplot(comptab, col=col)
```

## References
