Two-photon probes for pH: Detection of human colon cancer using two-photon microscopy.

2018 ◽  
Vol 36 (4_suppl) ◽  
pp. 607-607
Author(s):  
Woojung Kim ◽  
Eun Sun Kim ◽  
Geeho Min ◽  
Seung Han Kim ◽  
Seong ji Choi ◽  
...  

607 Background: In cancer cells, lysosomal pH decreases along with a concomitant increase in lysosomal volume and cathepsin expression levels. Lysosomes also play crucial roles in cancer progression following their release into the extracellular space. Since cancer cells invade a tissue by secreting degradative enzymes, the extracellular pH of tumor tissues becomes acidic. However, to date, there has been no report on the use of multi-photon microscopy (MPM) probes to image human colon cancer tissues. Methods: We have developed multi-photon (MP) pH-sensitive probes (BH-2 and BHEt-1) that exhibit absorption and emission maxima at 370 and 466 nm, and TP absorption cross-section values of 51 and 61 GM (1 GM = 10−50 cm4 s/photon), respectively, at 750 nm and pH 3.0 in a universal buffer (0.1 M citric acid, 0.1 M KH2PO4, 0.1 M Na2B4O7, 0.1 M Tris, 0.1 M KCl)/1,4-dioxane (7/ 3) solution. Results: The TPM images of CCD-18co (a normal colon cell line) and HCT116 cells (a colon cancer cell line) labeled with BH-2 were too dim to be distinguished. When the same cells were labeled with BHEt-1, however, the MPM image of the HCT116 cells was much brighter than that of CCD-18co cells, and the relative proportion of the acidic vesicles (Pacid) of the former was 5-fold larger than that of latter. BHEt-1 could also differentiate HepG2 cells (a human liver cancer cell line) from LX-2 cells (a human hepatic stellate cell line) with a 6-fold larger P acid value. Human colon cancer tissues labeled with BHEt-1 showed similar results, demonstrating much brighter MPM images and 6-fold larger Pacid values compared to normal tissue. Conclusions: These results suggest the potential utility of BHEt-1 for molecular image analysis of colon cancer tissues using MPM.

Oncogene ◽  
2001 ◽  
Vol 20 (35) ◽  
pp. 4884-4890 ◽  
Author(s):  
Duyen T Dang ◽  
Channing S Mahatan ◽  
Long H Dang ◽  
Iyabode A Agboola ◽  
Vincent W Yang

2016 ◽  
Vol 4 (3) ◽  
pp. 33-41 ◽  
Author(s):  
Huda A. Al Doghaither ◽  
Ayat B. Al-Ghafari ◽  
Sawsan A. Rahimulddin ◽  
Shiekhah M. Al Zahrani ◽  
Abdulkader M. Shaikh Omar ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
pp. 111
Author(s):  
Ladan Badiee Pourtaghi ◽  
Farahnaz Bineshian ◽  
Bizhan Sadighi Moghadam ◽  
Raheb Ghorbani ◽  
Hossein Nazari

Cancer is considered a serious threat to human health thatcolon cancer is the third most common cancer in the world. Colon cancer has undergone significant growth worldwide in recent years, and many people die every year as a result of this disease, which its treatment is a major challenge for researchers. In this study, we investigated the effect of anti-proliferative and apoptotic activity seed’s hydroalcoholic extract of Rumex obtusifolius, “is native to Semnan's northern region” on the human colon cancer cell line, SW480. The SW480 human colon cancer cell line were cultured in RPMI 1640 cell culture containing 10% Fetal bovine Serum and 1% Penicillin and Streptomycin antibiotics and incubated with a relative humidity of 95%, carbon dioxide 5% at 37°C. The SW480 cancer cell line was cultured in 48 and 96 well plates and treated with different concentrations of seeds hydroalcoholic extract of Rumex obtusifolius (20/40/80/160/320 micrograms/ml) for evaluation of cell viability by Trypan blue exclusion method and MTT assay. A non-treated group was used as control and a treated group with DMSO was used as solvent in solution of powdered extract as vehicle as well as positive control groups. Also, cell apoptosis assessment was performed by Propideum iodide/Annexin V test “Flowcytometry”and DNA fragmentation analysis “Agaros electrophoresis”. Seed hydroalcoholic extract caused cell death at concentrations of 40, 80, 160 and 320μg/ml, which the anticancer effect trend to increase significantly from 80μg/ml. The effect of R. obtusifolius seed extract even has more anti-cancer effect in 160 and 320μg/ml than cells which is treated to 5FU as a positive control groups. Seed hydroalcoholic extract reduced cell viability in proportion concentration. The effect of anticancer activity of seed extract trend to increase from 40μg/ml but it was shown effective concentrations for inhibiting of the cells growth were 160, 320μg/ml in 48 hr incubation time and 80, 160 and 320μg/ml in 72 hr incubation time. Also, the effect of this extract at concentrations of 160 and 320μg/ml with control group is not significant which have more cytotoxicity and even extract can have a significant effect on decreasing the survival of the SW480 cells. The data generated by flow cytometry are shown that colon cancer cells trend to necrosis and apoptotic pathway from 40μg/ml and increased significantly entrance to apoptotic pathway from 80μg/ml which is confirm the Trypan blue and MTT assay tests. Since the appearance of the DNA fragmentation, which precedes the bioavailability change, is characteristic to apoptosis, the extracts were considered to be apoptosis-inducers. The ability to inhibit growth and induction of apoptosis in SW480 cancer cells is a concentration- and time dependent manner. These results indicated that the induction of apoptosis at least partly mediates their cytotoxic activity which is necessary down further study for elucidation apoptotic signaling pathway.


2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Abdul Hakeem Memon ◽  
Zhari Ismail ◽  
Abdalrahim F. A. Aisha ◽  
Fouad Saleih Resq Al-Suede ◽  
Mohammad Shahrul Ridzuan Hamil ◽  
...  

Syzygium campanulatumKorth is an equatorial, evergreen, aboriginal shrub of Malaysia. Conventionally it has been used as a stomachic. However, in the currently conducted study dimethyl cardamonin or 2′,4′-dihydroxy-6′-methoxy-3′,5′-dimethylchalcone (DMC) was isolated fromS. campanulatumKorth, leaf extract. The structural characterization of DMC was carried out by making use of various techniques including UV, IR, NMR spectral followed by LC-MS, and X-ray crystallographic techniques. For determining the purity of compound, highly effective techniques including TLC, HPLC, and melting point were used. The cytotoxicity of DMC and three different extracts ofS. campanulatumwas evaluated against human colon cancer cell line (HT-29) by three different assays. DMC and ethanolic extract revealed potent and dose-dependent cytotoxic activity on the cancer cell line with IC5012.6 and 90.1 µg/mL, respectively. Quite astonishingly to our knowledge, this is the very first report onS. campanulatumas being a rich source (3.5%) of DMC, X-ray crystallography, and anticancer activity on human colon cancer cells.


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