Involvement of mitochondrial intrinsic pathway in rhSP-D (recombinant human Surfactant Protein D) induced apoptosis of prostate cancer cells
Bibliographic record
Abstract
Surfactant protein D (SP-D), an innate immune molecule, has an indispensable role in host defense and regulation of inflammation. We reported a novel anti-cancer role of a recombinant fragment of human SP-D (rhSP-D) in leukemic and breast tumor cell lines. A recent study revealed correlation of SP-D expression in Prostate cancer tissues with increased Gleason score and tumor volume. In the present study, we elucidated the role of rhSP-D in prostate cancer using LNCaP (androgen dependent), PC3 (androgen independent) cell lines and primary prostate cancer cells. In accordance with our previous finding, rhSP-D induced apoptosis in LNCaP and PC3 cell lines in a time and dose dependent manner. Isolated primary prostate cancer epithelial cells from explant cultures of tissue biopsies of prostate cancer patients were characterised for the presence of Cytokeratin (epithelial cell), CD10 (negative) and CD164 (positive) markers at protein and transcript level. Anti-prostate tumor effect of rhSP-D was established in the isolated primary prostate cancer epithelial cells. Importantly, primary normal prostate epithelial cells treated with similar concentrations of rhSP-D showed no adverse effect on viability. rhSP-D upregulated phospho p53 and transcripts of Bax and reduced Bcl2 transcripts, suggesting p53 mediated apoptosis in LNCaP cells. rhSP-D induced apoptosis in PC3 cells by lowering phospho ERK1/2 levels and increased BAD transcripts, a distinct mechanism of programmed cell death. Increased release of cytochrome c upon rhSP-D confirmed the activation of mitochondrial intrinsic apoptotic pathway in both the cell types. rhSP-D treatment downregulated transcripts of Bcl2 while upregulated PUMA transcripts, suggesting p53 mediated apoptosis primary prostate cancer cells. Also, positive TUNEL assay confirmed induction of apoptosis by rhSP-D in cancer tissue biopsies. Collectively, our findings reveal an integral role of SP-D in immune surveillance against prostate cancer mediated by two distinct mitochondrial apoptotic mechanisms.
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.000 | 0.000 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.001 | 0.000 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".