今天嘗試復(fù)現(xiàn)兩種常見實驗圖表——細胞生長曲線與腫瘤生長曲線。在R中,我們可以通過ggplot2繪制帶誤差棒的折線圖+散點圖來實現(xiàn)我們的可視化需求。在繪制生長曲線圖中,需要注意以下幾點:


1、橫軸通常表示時間,可以是天、周、月等時間單位,也可能是給藥濃度/劑量等。


2、腫瘤生長曲線縱軸表示腫瘤的體積、質(zhì)量或大小,細胞生長曲線縱軸表示細胞的相對數(shù)量,不同的實驗方法標注截然不同。


3、每個組別的生長曲線通常會以不同的線條或顏色表示,如果組別較多,加之需要添加error bar,組別的顏色需要仔細選擇以便區(qū)分。


A、細胞生長曲線


細胞生長曲線是測定細胞絕對生長數(shù)的常用方法,也是判定細胞活力的重要指標,它以培養(yǎng)時間為橫坐標,細胞密度為縱坐標。這里復(fù)現(xiàn)nature cancer上面一篇文章的Fig2e:


Network-based assessment of HDAC6 activity predicts preclinical and clinical responses to the HDAC6 inhibitor ricolinostat in breast cancer.Nat Cancer.2023 Feb;2022 Dec 30.PMID:36585452.

Growth curves of sensitive(S)vs resistant(R)BC cells treated with four different HDAC6 inhibitors(n=3 independent experiments/per drug concentration).All error bars represent Mean±SD.P value was estimated by two-tailed t test.


library(readxl)

library(tidyverse)

##數(shù)據(jù)整理:ggplot2所需畫圖格式

Mean <- data.frame(read_excel("./Fig1e.xlsx", sheet = "Mean",na = "NA"))

Mean <- reshape2::melt(Mean[,-1])

StDev <- data.frame(read_excel("./Fig1e.xlsx", sheet = "St. Dev",na = "NA"))

StDev <- reshape2::melt(StDev[,-1])


Scatter <- data.frame(Mean = Mean$value,

                     SD =  StDev$value,

                     Con = rep(c("0","0.3125","0.625","1.25","2.5","5","10"),each = 4))

Scatter$Group <- rep(c("MDA-MB-453","SKBR3","MDA-MB-436","MDA-MB-468"),7)

Scatter$Group <- factor(Scatter$Group,levels = c("MDA-MB-453","SKBR3","MDA-MB-436","MDA-MB-468"))

Scatter$Con <- factor(Scatter$Con,levels = c("0","0.3125","0.625","1.25","2.5","5","10"))


library(ggplot2)

theme <- theme(plot.title = element_text(hjust = 0.5,size = 22),

              plot.margin = margin(0.5,0.5,0.5,0.5,unit = "cm"),#設(shè)置畫板邊緣大小

              axis.text.x = element_text(hjust = 0.5,size = 18),

              axis.text.y = element_text(hjust = 0.5,size = 18),

              axis.title.y = element_text(size = 18),

              axis.title.x = element_text(size = 18),

              legend.text = element_text(size = 18),

              legend.title = element_blank(),

              legend.position = c(0.2,0.2),

              legend.key.width = unit(1,"cm"),#圖例寬度

              legend.key.height = unit(1,"cm"),#圖例高度

              legend.background = element_blank())


Fig_1e <- ggplot(Scatter,aes(x = Con,y = Mean,color = Group,group = Group)) +

         geom_errorbar(aes(ymin = Mean - SD,ymax = Mean + SD),color = "black",width = 0.2) +

         geom_point(size = 3) +

         geom_line(linewidth = 1.5) +

         labs(x = "concentration(μM)",y = "% Cell Number",title = "Ricolinostat") +

         scale_y_continuous(limits = c(0,120),breaks = seq(0,120,20),expand = c(0,0)) +

         scale_color_manual(values = c("#982b2b","#db6968","#88c4e8","#005496")) +

         theme_classic() +

         theme

Fig_1e


B、腫瘤生長曲線


腫瘤生長曲線圖是一種用于描述腫瘤體積、質(zhì)量或大小隨時間變化的圖表。這種圖表通常用于研究腫瘤在不同治療條件下的生長情況,或者用于比較不同腫瘤類型之間的生長速率。同樣復(fù)現(xiàn)nature cancer上面一篇文章的Fig2a:


Interleukin 17 signaling supports clinical benefit of dual CTLA-4 and PD-1 checkpoint inhibition in melanoma.Nat Cancer.2023 Sep;4(9):1292-1308.Nat Cancer.2023 Aug 14;PMID:37525015.

a,Tumor growth kinetics of transplanted CM(BRAF-WT ICI-sensitive)melanoma tumors treated with immunoglobulin G(IgG)or H2O(control),anti-CTLA-4+anti-PD-1,anti-CTLA-4+anti-PD-1+rm-IL-17A and anti-CTLA-4+anti-PD-1+α-IL-17A antibodies according to the depicted treatment schedule.Data points show mean+s.e.m.until the day when the first mice were eliminated from each group.


library(readxl)

library(tidyverse)

##數(shù)據(jù)整理:ggplot2所需畫圖格式

Scatter <- read_excel("./Fig-supp.xlsx", sheet = "Fig.2a",na = "NA",skip = 2)

Scatter <- rbind(rbind(as.matrix(Scatter[,1:4]),as.matrix(Scatter[,c(1,5:7)])),

                rbind(as.matrix(Scatter[,c(1,8:10)]),as.matrix(Scatter[,c(1,11:13)])))

colnames(Scatter) <- c("Day","Mean","SEM","N")

Scatter <- data.frame(Scatter)

Scatter$Group <- rep(c("Control (IgG/H2O)",

                      "α-CTLA-4+α-PD-1",

                      "α-CTLA-4+α-PD-1+rm IL-17A",

                      "α-CTLA-4+α-PD-1+α-IL-17A"),

                    each = 20)

Scatter$Group <- factor(Scatter$Group,levels = unique(Scatter$Group))

Scatter$SEM <- ifelse(Scatter$Mean == 0,0,Scatter$SEM)

#  Day Mean  SEM N             Group

#1   8 25.8  5.0 3 Control (IgG/H2O)

#2   9 46.0 10.0 4 Control (IgG/H2O)

#3  10 46.0 10.0 4 Control (IgG/H2O)

#4  11 55.6 16.3 5 Control (IgG/H2O)

#5  12 84.9 16.2 6 Control (IgG/H2O)

#6  13 92.1 14.4 6 Control (IgG/H2O)

library(ggplot2)

theme <- theme(plot.title = element_text(hjust = 0.5,size = 22),

              plot.margin = margin(0.5,0.5,0.5,0.5,unit = "cm"),#設(shè)置畫板邊緣大小

              axis.text.x = element_text(hjust = 0.5,size = 18),

              axis.text.y = element_text(hjust = 0.5,size = 18),

              axis.title.y = element_text(size = 18),

              axis.title.x = element_text(size = 18),

              legend.text = element_text(size = 18),

              legend.title = element_blank(),

              legend.position = "right",

              legend.key.width = unit(1,"cm"),#圖例寬度

              legend.key.height = unit(1,"cm"),#圖例高度

              legend.background = element_blank())


Fig_2a <- ggplot(Scatter,aes(x = Day,y = Mean,color = Group,group = Group)) +

         geom_errorbar(aes(ymin = Mean,ymax = Mean + SEM),color = "grey",width = 0.4) + #僅展示上半部分

         geom_point(size = 5) +

         geom_line(linewidth = 2.5) +

         labs(x = "Time (d)",y = expression("Tumor volume (mm"^3*")")) +

         scale_x_continuous(limits = c(8,28),breaks = seq(8,28,4),expand = c(0,0)) +

         scale_y_continuous(limits = c(0,1250),breaks = seq(0,1250,250),expand = c(0,0)) +

         scale_color_manual(values = c("black","#1b6292","#ff8080","#c5934e")) +

         theme_classic() +

         theme

Fig_2a


組間比較統(tǒng)計結(jié)果可以在AI或PS里面添加。


相關(guān)新聞推薦

1、在非常低的抗生素濃度下選擇耐藥性細菌:討論、材料和方法

2、照光對稻曲病菌菌絲生長的影響與調(diào)控機制(一)

3、單細胞微生物生長時期精準鑒定與實時監(jiān)測方法(二)

4、十二酸單甘油酯對PEDV感染3D4/21巨噬細胞活性、基因表達的影響(三)

5、重金屬抗性菌CL01促進紫云英抵抗銅脅迫機理