Two human-derived CRC cell lines LOVO (CCL-229) and HCT-8 (CCL-244) were obtained from the American Type Culture Collection (Manassas, VA, USA) and cultured with RPMI-1640 (Invitrogen; Thermo Fisher Scientific, Inc., Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS; Invitrogen), 100 U/ml penicillin and 100 mg/ml streptomycin (Thermo Fisher Scientific, Inc., Waltham, MA, USA) in 5% CO₂ at 37°C.

Total RNA from cells was isolated using TRIzol reagent (Invitrogen) according to the manufacturer's directions. Then, 1 µg total RNA was used for reverse transcription reaction using SuperScript III reverse transcriptase (Invitrogen). qPCR was performed using an ABI 7500 real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc., Foster City, CA, USA), and the mRNA expression of human KLK11 and β-actin was evaluated using a LightCycler Fast Start DNA Master SYBR Green I kit (Roche Diagnostics GmbH, Mannheim, Germany). PCR amplification was performed by denaturation at 95°C for 10 min, annealing and extension at 60°C for 60 sec for 40 cycles. RT-qPCR analysis was performed using the following primers: KLK11 forward: 5′-GTTCGAGAAGACGCGGCTAC-3′; KLK11 reverse: 5′-GGTGGGAGAGGTGAGTGAC-3′. β-actin forward: 5-CCA ACC GCG AGA AGA TGA-3′; β-actin reverse: 5′-CCAGAGGCGTACAGGGATAG-3′. The relative expression level of KLK11 was calculated using the ΔΔCq method (21) and normalized against that of β-actin. All PCR amplification was performed in triplicate and repeated in three independent experiments.

In order to silencing KLK11, the short hairpin RNA (shRNA) were generated by ligating synthetic oligonucleotides (Invitrogen) against the target genes into the AgeI and EcoRI sites of pLKO.1-TRC cloning vector (provided by Dr Xuchao Zhu; Tenth People's Hospital, Affiliated to Tongji University, Shanghai, China). The sequences of the KLK11 shRNA (shKLK11) and shRNA control (SCR) were as follows: KLK11-SH1 sense, 5′-CCGGCCAACAACAACCACCGCAATGCTCGCACATTGCGGTGGTCTTTGTTGGTTTTTG-3′ and antisense, 5′-AATTCAAAAACCAACAACAACCACCGCAATGCTCGCACATTGCGGTGGTCTTTGTTGG-3′; KLK11-SH2 sense, 5′-CCGGGCAATGCTGTCACTTAATAATCTCGCAATTATTACATGACCACATCTCTTTTTG-3′ and antisense, 5′-AATTCAAAAAGCAATGCTGTCACTTAATAATCTCGCAATTATTACATGACCACATCTC-3′; KLK11-SH3 sense, 5′-CCGGCTGGTCTGTAACCCATCTCTTCTCGCAACAAGACTGGTTACAGACCCATTTTTG-3′ and antisense, 5′-AATTCAAAAACTGGTCTGTAACCCATCTCTTCTCGCAACAAGACTGGTTACAGACCAG-3′; control shRNA sense, 5′-CCGGAAACTACCGTTGTTATCAGTGTTCACAAGACACCTATAACAACGGTCATTTTTTTTG-3′ and antisense, 5′-AATTCAAAAAAAACTACCGTTGTTATCAGTGTCTCTTGAACACCTATAACAACGGTCATTT-3′. Lentiviral virions were produced by co-transfection of HEK293T cells with 5 µg pLKO.1-puro vector and 5 µg packaging and envelope vectors using Lipofectamine 2000 (Invitrogen) according to the manufacturer's protocol. Lentivirus was harvested 48 h after transfection. LOVO and HCT-8 cells were infected with lentivirus containing shKLK11 or SCR for 24 h. Two days later, the virus-infected cells were selected by 2 µg/ml puromycin (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) for 48 h and subjected to required assays.

Cell viability was quantified using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay as previously described (22). Briefly, 3×10³ transiently transfected LOVO and HCT-8 cells (SCR or shKLK11) were seeded in 96-well plates and 20 µl MTT solution (5 mg/ml; Sigma-Aldrich) was added to each well 72 and 96 h later. The optical density was measured using a microplate reader (Bio-Rad Laboratories, Inc., Hercules, CA, USA) at 595 nm.

For drug sensitivity, cells were plated in 96-well plates at 5×10⁴ cells per well, followed by treatment with 0, 5 or 10 µmol/lL-OHP for 24 h. The optical density was then measured and the cell viability was calculated.

Apoptosis detection was performed using an Annexin V Apoptosis Detection kit I (BD Biosciences, Franklin Lakes, NJ, USA). In brief, cells were collected and washed with phosphate-buffered saline (PBS). Then, 5 µl annexin V and propidium iodide was added to the cell suspension and incubated at room temperature in the dark for 30 min. The volume was then made up to 500 µl and the cells were analyzed using a FACSCalibur flow cytometer (BD Biosciences).

The activity of caspase-3 was measured using a Caspase-3 Assay kit (Abnova Corporation, Taipei, Taiwan) according to the manufacturer's instructions. In brief, 5×10⁶ cells were harvested, resuspended in 50 µl chilled cell lysis buffer and incubated on ice for 10 min. Then, 50 µl 2.0X Reaction Buffer was added to each sample, along with 5 µl DEVD-pNA (4 mM) substrate and incubated for 2 h at 37°C. The optical density was measured at 405 nm using a microplate reader (Bio-Rad Laboratories, Inc.).

Cell lysates were prepared in a buffer containing 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1% NP-40 (v/v) and 150 mM NaCl, supplemented with a mixture of complete protease inhibitors (Roche Diagnostics, Basel, Switzerland). Equal quantities of protein (40 µg) were then separated on 10% SDS-PAGE and blotted onto a polyvinylidene difluoride membrane (Bio-Rad Laboratories, Inc.). Blocking was performed at room temperature using Tris-buffered saline with 0.1% Tween-20 (TBST; J&K Chemical Ltd., Shanghai, China) containing 5% non-fat milk for 1 h. The membrane was then incubated with primary mouse monoclonal KLK11 antibody (sc-20387; 1:500) and rabbit polyclonal β-actin (sc-47778; 1:1,000; Santa Cruz Biotechnology, Inc., Dallas, TX, USA), Bcl-2 (#2872; 1:1,000) and Bax (#2772; 1:1,000) antibodies (Cell Signaling Technology, Inc., Danvers, MA, USA) in TBST at 4°C overnight and with the appropriate horseradish peroxidase-conjugated secondary antibody (CW0103M; 1:3000; CWbiotech, Beijing, China) for 1 h at room temperature. Specific antibody binding was detected using an ECL system (GE Healthcare, Piscataway, NJ, USA).

Data are presented as the mean ± standard deviation. Statistical analysis was performed using SPSS software, version 16.0 (SPSS, Inc., Chicago, IL, USA). Statistical significance was considered to be indicated by P<0.05.

A previous study has shown that the expression of KLK11 was upregulated in colorectal tumors (18). To determine whether KLK11 is involved in the progression of CRC, three different lentivirus-based shRNAs (KLK11 SH1, KLK11 SH2 and KLK11 SH3) were employed to downregulate KLK11 expression. The mRNA and protein levels of KLK11 in stably transfected LOVO and HCT-8 cells were confirmed using RT-qPCR and western blot analysis (Fig. 1). The mRNA expression levels of KLK11 were significantly decreased in KLK11 SH3 groups in both cell lines. The subsequent assays were performed with KLK11 SH3, which is furthermore referred to as shKLK11. These results suggested that the lentivirus-mediated shRNA targeting KLK11 could effectively knockdown KLK11 expression in CRC cells.

To determine the biological function of KLK11 in CRC progression, MTT assays were used to examine the proliferative ability of CRC cells. As shown in Fig. 2A and B, the proliferation rates of shKLK11-infected cells started to decrease and were reduced compared with those of the SCR groups on days 3 and 4.

There is considerable evidence indicating that apoptosis has a close association with cell growth (23). In the present study, apoptosis assays were performed using CRC cells following KLK11 silencing. The results of flow cytometric analysis indicated that the percentages of apoptotic cells were significantly increased in shKLK11-infected LOVO and HCT-8 cells compared with the respective SCR groups (Fig. 2C and D). This finding indicated that KLK11 may serve a crucial function in the proliferation and tumorigenesis of CRC cells in vitro.

To examine the mechanism underlying the inhibition of cell growth, the expression of Bcl-2 and Bax, two important proteins of the apoptosis signaling pathway (24) was investigated. Western blot analysis showed that knockdown of KLK11 lead to a reduction of Bcl-2 and an increase of Bax in both cell lines (Fig. 3A). Caspase-3, a crucial mediator of apoptosis, is a frequently activated death protease, catalyzing the specific cleavage of various key cellular proteins (25). A significant increase in caspase-3 activity was detected in shKLK11-infected LOVO and HCT-8 cells compared with SCR groups (Fig. 3B). Collectively, these data demonstrated that the proliferative effect of KLK11 in CRC cells is regulated via the apoptosis pathway.

Our previous study has shown that dysregulation of KLK11 expression had an association with FOLFOX4 chemotherapy in human CRC cells (26). However, whether KLK11 played a key role in affecting the sensitivity of CRC cells was not fully understood. To elaborate on this, LOVO and HCT-8 cells with stable KLK11 silencing were treated with 0, 5 or 10 µmol/l L-OHP for 24 h. The results of MTT assay suggested that knockdown of KLK11 led to a significant reduction in the viability of CRC cells in response to L-OHP in a dose-dependent manner compared with control (Fig. 4A and B). Furthermore, flow cytometric analysis showed that the apoptotic rate of cells with stable KLK11 silencing treated with L-OHP was significantly higher than that of cells treated with control (Fig. 4C and D). Collectively, these results suggest that knockdown of KLK11 could increase the chemosensitivity of CRC cells to L-OHP by inducing apoptosis enhancement in vitro.