人转移胰腺腺癌细胞 disease models

AsPC-1 (Pancreatic ductal adenocarcinoma). Standardized family protocols with foolproof steps, flowcharts, and methodology PubMed refs—optimize per datasheet and pilots. Research use only (RUO).

Adapted from PubMed literature for research use only (RUO); adjust per lab SOP and pilots.

Use case

Use AsPC-1 in 2D culture to test how compounds or genetic perturbations affect proliferation/survival—baseline solid-tumor readout.

In one line

Stable culture → seed overnight → dose matrix → timed viability/apoptosis → compare vs vehicle.

Protocol overview

01
Expand; log passage
02
Seed plates to assay density
03
Attach / stabilize overnight
04
Add dose matrix + vehicle
05
Incubate to endpoint
06
Viability / apoptosis assay
07
Compute IC₅₀ or % inhibition

01[Prep] Confirm complete medium per datasheet; mycoplasma-negative before key assays.
02[Seed] Count and plate so cultures are ~40–70% confluent at dosing; overnight for adherent lines.
03[Dose] Vehicle + ≥5-point log dose grid; optional cytotoxic positive control. Keep DMSO ≤0.1–0.5% if possible.
04[Incubate] Typically 24–72 h; minimize disturbance.
05[Viability] MTT / CCK-8 / CellTiter-Glo per kit; ≥3 wells/group.
06[Optional apoptosis] Annexin V / caspase or DNA fragmentation.
07[Optional colony] Low-density plating, 1–3 weeks, crystal violet colony counts.
08[Calculate] % inhibition vs vehicle; fit IC₅₀; ≥2–3 independent repeats.
09[QC] Log passage and serum lot; exclude contaminated/detached wells.

Reagents / compounds

Name	Role	Conc.
Test compound / inhibitor	Drug response or pathway intervention	对数梯度；按文献与预实验优化
Vehicle control (e.g. DMSO)	Rule out vehicle artifacts	与最高药组等体积分数
Viability reagent (MTT / CCK-8 / CTG)	Quantify viability/metabolic activity	按试剂盒说明书

Readouts

(1) Viability / IC₅₀; (2) optional apoptosis; (3) optional colonies; (4) morphology.

Literature & manuals

[1]PubMedPMID 1630814Oncogene · 1992
Human pancreatic carcinomas and cell lines reveal frequent and multiple alterations in the p53 and Rb-1 tumor-suppressor genes.
[2]PubMedPMID 1764370British journal of cancer · 1991
Abnormalities of the p53 tumour suppressor gene in human pancreatic cancer.
[3]PubMedPMID 6606682J Immunol Methods · 1983
Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays.
[4]PubMedPMID 16740937Nat Protoc · 2006
Clonogenic assay of cells in vitro.
[5]PubMedPMID 2135685J Exp Med · 1990
Early redistribution of plasma membrane phosphatidylserine is a general feature of apoptosis.

Use case

Assess horizontal migration or matrix invasion of AsPC-1 for metastasis-related mechanisms and anti-migratory screens.

In one line

Confluent scratch or Transwell seeding → treat → timed imaging / count invaded cells.

Protocol overview

01
Seed to confluence or Transwell
02
Scratch or add invasion matrix
03
Switch to drug + low-serum medium
04
Timed imaging / stain membrane
05
Quantify wound area or invaded cells
06
Compare vs vehicle

Reagents / compounds

Name	Role	Conc.
Low-serum medium	Reduce proliferation confounders	常用 0.5–2% FBS（按 SOP）
Matrigel / invasion matrix (optional)	Model ECM invasion	按说明书稀释铺胶
Test compound / inhibitor	Drug response or pathway intervention	对数梯度；按文献与预实验优化
Vehicle control (e.g. DMSO)	Rule out vehicle artifacts	与最高药组等体积分数

Readouts

(1) Wound closure; (2) invaded cell counts; (3) paired viability.

Literature & manuals

[1]PubMedPMID 1630814Oncogene · 1992
Human pancreatic carcinomas and cell lines reveal frequent and multiple alterations in the p53 and Rb-1 tumor-suppressor genes.
[2]PubMedPMID 1764370British journal of cancer · 1991
Abnormalities of the p53 tumour suppressor gene in human pancreatic cancer.
[3]PubMedPMID 17546025Cell Adh Migr · 2007
An introduction to the wound healing assay using live-cell microscopy.
[4]PubMedPMID 22130855J Vis Exp · 2011
In vitro cell migration and invasion assays.

Use case

Fix passage window and mycoplasma/morphology baselines to reduce lot drift.

In one line

Log thaw passage → mycoplasma check → archive morphology → run key assays in-window.

Protocol overview

01
Thaw & log passage
02
Mycoplasma check
03
Archive morphology
04
Run key assays in window

Readouts

Mycoplasma-negative, stable morphology, in-window passage, viability baseline.

Literature & manuals

[1]PubMedPMID 1630814Oncogene · 1992
Human pancreatic carcinomas and cell lines reveal frequent and multiple alterations in the p53 and Rb-1 tumor-suppressor genes.
[2]PubMedPMID 1764370British journal of cancer · 1991
Abnormalities of the p53 tumour suppressor gene in human pancreatic cancer.

Pancreatic ductal adenocarcinoma-related 2D viability / drug screen — foolproof protocol

Use case

In one line

Foolproof steps (9)

Reagents / compounds

Readouts

Literature & manuals

Migration / invasion — foolproof protocol (scratch or Transwell)

Use case

In one line

Foolproof steps (8)

Reagents / compounds

Readouts

Literature & manuals

Passage-window & QC checklist

Use case

In one line

Foolproof steps (6)

Readouts

Literature & manuals